Linked Data
ClinVar Variation Id:
337276
dbSNP Id:
rs147427088
ExAC:
2:85787954 G / A
gnomAD v2:
2-85787954-G-A
gnomAD v3:
2-85560831-G-A
gnomAD v4:
2-85560831-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.85560831G>A , CM000664.2:g.85560831G>A | GRCh38 |
| NC_000002.11:g.85787954G>A , CM000664.1:g.85787954G>A | GRCh37 |
| NC_000002.10:g.85641465G>A | NCBI36 |
| NG_011811.2:g.5704C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000482662.2:n.265C>T | ||
| ENST00000496962.2:c.198C>T | ENSP00000508856.1:p.Val66= | |
| ENST00000685865.1:n.290C>T | ||
| ENST00000687250.1:n.301C>T | ||
| ENST00000687995.1:n.239C>T | ||
| ENST00000688205.1:c.198C>T | ENSP00000509673.1:p.Val66= | |
| ENST00000688788.1:n.290C>T | ||
| ENST00000689276.1:c.198C>T | ENSP00000510012.1:p.Val66= | |
| ENST00000689576.1:c.198C>T | ENSP00000508712.1:p.Val66= | |
| ENST00000690108.1:c.198C>T | ENSP00000510617.1:p.Val66= | |
| ENST00000690468.1:c.43+555C>T | ENSP00000509078.1:n.43+555C>T | |
| ENST00000690595.1:c.198C>T | ENSP00000508979.1:p.Val66= | |
| ENST00000691348.1:c.43+555C>T | ENSP00000509369.1:n.43+555C>T | |
| ENST00000691410.1:c.198C>T | ENSP00000508479.1:p.Val66= | |
| ENST00000693287.1:c.-67+555C>T | ENSP00000510264.1:n.-67+555C>T | |
| ENST00000693681.1:c.43+555C>T | ENSP00000510789.1:n.43+555C>T | |
| ENST00000233838.9:c.198C>T MANE Select | ENSP00000233838.3:p.Val66= | |
| ENST00000233838.8:c.198C>T | ENSP00000233838.3:p.Val66= | |
| ENST00000421496.5:c.43+555C>T | ENSP00000400384.1:n.43+555C>T | |
| ENST00000423570.5:c.198C>T | ENSP00000389426.1:p.Val66= | |
| ENST00000428479.3:c.43+555C>T | ENSP00000390748.3:n.43+555C>T | |
| ENST00000430215.7:c.43+555C>T | ENSP00000408045.3:n.43+555C>T | |
| ENST00000465637.5:n.108+555C>T | ||
| ENST00000481541.1:n.108+555C>T | ||
| ENST00000496962.1:n.317C>T | ||
| NM_000821.5:c.198C>T | NP_000812.2:p.Val66= | |
| NM_000821.6:c.198C>T | NP_000812.2:p.Val66= | |
| NM_001142269.2:c.43+555C>T | NP_001135741.1:n.43+555C>T | |
| NM_001142269.3:c.43+555C>T | NP_001135741.1:n.43+555C>T | |
| NM_001311312.1:c.198C>T | NP_001298241.1:p.Val66= | |
| XM_005264259.3:c.198C>T | XP_005264316.1:p.Val66= | |
| XM_011532764.1:c.-461C>T | XP_011531066.1:n.-461C>T | |
| XM_011532765.1:c.-445+555C>T | XP_011531067.1:n.-445+555C>T | |
| XR_939677.1:n.263C>T | ||
| XM_005264259.5:c.198C>T | XP_005264316.1:p.Val66= | |
| XM_011532764.3:c.-461C>T | XP_011531066.1:n.-461C>T | |
| XM_011532765.3:c.-445+555C>T | XP_011531067.1:n.-445+555C>T | |
| XM_017003803.2:c.43+555C>T | XP_016859292.1:n.43+555C>T | |
| XR_001738703.2:n.263C>T | ||
| NM_000821.7:c.198C>T MANE Select | NP_000812.2:p.Val66= | |
| NM_001142269.4:c.43+555C>T | NP_001135741.1:n.43+555C>T | |
| NM_001311312.2:c.198C>T | NP_001298241.1:p.Val66= |