Linked Data
ClinVar Variation Id:
324190
dbSNP Id:
rs746826852
ExAC:
17:57079017 A / G
gnomAD v2:
17-57079017-A-G
gnomAD v3:
17-59001656-A-G
gnomAD v4:
17-59001656-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.59001656A>G , CM000679.2:g.59001656A>G | GRCh38 |
| NC_000017.10:g.57079017A>G , CM000679.1:g.57079017A>G | GRCh37 |
| NC_000017.9:g.54433799A>G | NCBI36 |
| NG_009298.1:g.110250T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262294.12:c.2754T>C MANE Select | ENSP00000262294.7:p.His918= | |
| ENST00000262294.11:c.2754T>C | ENSP00000262294.7:p.His918= | |
| ENST00000393065.6:c.2652T>C | ENSP00000376784.2:p.His884= | |
| ENST00000393066.7:c.2754T>C | ENSP00000376785.3:p.His918= | |
| ENST00000577554.5:c.*2568-2197T>C | ENSP00000462340.1:n.*2568-2197T>C | |
| ENST00000583945.5:c.81-2197T>C | ||
| ENST00000585287.5:c.213T>C | ENSP00000464666.1:p.His71= | |
| NM_001005207.2:c.2754T>C | NP_001005207.1:p.His918= | |
| NM_015294.3:c.2754T>C | NP_056109.1:p.His918= | |
| XM_005257385.1:c.2781T>C | XP_005257442.1:p.His927= | |
| XM_005257387.1:c.2652T>C | XP_005257444.1:p.His884= | |
| XM_005257389.1:c.2696-2197T>C | XP_005257446.1:n.2696-2197T>C | |
| XM_005257390.1:c.2696-2197T>C | XP_005257447.1:n.2696-2197T>C | |
| XM_011524831.1:c.2781T>C | XP_011523133.1:p.His927= | |
| XM_011524832.1:c.2754T>C | XP_011523134.1:p.His918= | |
| XM_011524833.1:c.2730T>C | XP_011523135.1:p.His910= | |
| XM_011524834.1:c.2679T>C | XP_011523136.1:p.His893= | |
| XM_011524835.1:c.2652T>C | XP_011523137.1:p.His884= | |
| XM_011524836.1:c.2696-2197T>C | XP_011523138.1:n.2696-2197T>C | |
| XM_011524837.1:c.*53T>C | XP_011523139.1:n.*53T>C | |
| NM_001005207.4:c.2754T>C | NP_001005207.1:p.His918= | |
| NM_001320987.2:c.2652T>C | NP_001307916.1:p.His884= | |
| NM_001320988.2:c.2696-2197T>C | NP_001307917.1:n.2696-2197T>C | |
| NM_001320989.2:c.2696-2197T>C | NP_001307918.1:n.2696-2197T>C | |
| NM_001320990.2:c.2330-2197T>C | NP_001307919.1:n.2330-2197T>C | |
| NM_001353082.1:c.2679T>C | NP_001340011.1:p.His893= | |
| NM_001353083.1:c.2019T>C | NP_001340012.1:p.His673= | |
| NM_001353084.1:c.2781T>C | NP_001340013.1:p.His927= | |
| NM_001353085.1:c.2292T>C | NP_001340014.1:p.His764= | |
| NM_001353086.1:c.2703T>C | NP_001340015.1:p.His901= | |
| NM_015294.5:c.2754T>C | NP_056109.1:p.His918= | |
| NR_148346.1:n.3298T>C | ||
| NR_148347.1:n.3196T>C | ||
| XM_011524832.2:c.2754T>C | XP_011523134.1:p.His918= | |
| XM_017024662.1:c.2781T>C | XP_016880151.1:p.His927= | |
| XM_017024663.2:c.2754T>C | XP_016880152.1:p.His918= | |
| XM_017024664.1:c.2730T>C | XP_016880153.1:p.His910= | |
| XM_017024665.1:c.2652T>C | XP_016880154.1:p.His884= | |
| XM_017024667.1:c.2703T>C | XP_016880156.1:p.His901= | |
| XM_017024669.2:c.2601T>C | XP_016880158.1:p.His867= | |
| XM_017024670.2:c.2594-2197T>C | XP_016880159.1:n.2594-2197T>C | |
| XM_017024671.2:c.2292T>C | XP_016880160.1:p.His764= | |
| XM_017024672.1:c.2234-2197T>C | XP_016880161.1:n.2234-2197T>C | |
| XM_017024673.2:c.2046T>C | XP_016880162.1:p.His682= | |
| XM_024450765.1:c.2292T>C | XP_024306533.1:p.His764= | |
| NM_015294.6:c.2754T>C MANE Select | NP_056109.1:p.His918= | |
| NM_001005207.5:c.2754T>C | NP_001005207.1:p.His918= | |
| NM_001320987.3:c.2652T>C | NP_001307916.1:p.His884= | |
| NM_001320988.3:c.2696-2197T>C | NP_001307917.1:n.2696-2197T>C | |
| NM_001320989.3:c.2696-2197T>C | NP_001307918.1:n.2696-2197T>C | |
| NM_001320990.3:c.2330-2197T>C | NP_001307919.1:n.2330-2197T>C | |
| NM_001353082.2:c.2679T>C | NP_001340011.1:p.His893= | |
| NM_001353083.2:c.2019T>C | NP_001340012.1:p.His673= | |
| NM_001353084.2:c.2781T>C | NP_001340013.1:p.His927= | |
| NM_001353085.2:c.2292T>C | NP_001340014.1:p.His764= | |
| NM_001353086.2:c.2703T>C | NP_001340015.1:p.His901= | |
| NR_148346.2:n.3214T>C | ||
| NR_148347.2:n.3112T>C |