Linked Data
dbSNP Id:
rs1162815494
gnomAD v2:
18-31323889-G-C
gnomAD v3:
18-33743925-G-C
gnomAD v4:
18-33743925-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.33743925G>C , CM000680.2:g.33743925G>C | GRCh38 |
| NC_000018.9:g.31323889G>C , CM000680.1:g.31323889G>C | GRCh37 |
| NC_000018.8:g.29577887G>C | NCBI36 |
| NG_055244.1:g.170349G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696964.1:c.4080G>C | ENSP00000513003.1:p.Leu1360Phe | |
| ENST00000269197.12:c.4077G>C MANE Select | ENSP00000269197.4:p.Leu1359Phe | |
| ENST00000681521.1:c.3957G>C | ENSP00000506037.1:p.Leu1319Phe | |
| ENST00000269197.9:c.4077G>C | ENSP00000269197.4:p.Leu1359Phe | |
| NM_030632.1:c.4077G>C | NP_085135.1:p.Leu1359Phe | |
| XM_005258356.1:c.4080G>C | XP_005258413.1:p.Leu1360Phe | |
| XM_011526205.1:c.4053G>C | XP_011524507.1:p.Leu1351Phe | |
| XM_011526206.1:c.3999G>C | XP_011524508.1:p.Leu1333Phe | |
| XM_011526207.1:c.3999G>C | XP_011524509.1:p.Leu1333Phe | |
| XM_011526208.1:c.3960G>C | XP_011524510.1:p.Leu1320Phe | |
| XM_011526209.1:c.3909G>C | XP_011524511.1:p.Leu1303Phe | |
| XM_011526210.1:c.3909G>C | XP_011524512.1:p.Leu1303Phe | |
| XM_011526211.1:c.3909G>C | XP_011524513.1:p.Leu1303Phe | |
| XM_011526212.1:c.3909G>C | XP_011524514.1:p.Leu1303Phe | |
| XM_011526213.1:c.3909G>C | XP_011524515.1:p.Leu1303Phe | |
| XM_011526214.1:c.3909G>C | XP_011524516.1:p.Leu1303Phe | |
| XM_011526215.1:c.1041G>C | XP_011524517.1:p.Leu347Phe | |
| NM_030632.2:c.4077G>C | NP_085135.1:p.Leu1359Phe | |
| XM_011526205.2:c.4053G>C | XP_011524507.1:p.Leu1351Phe | |
| XM_011526206.2:c.3999G>C | XP_011524508.1:p.Leu1333Phe | |
| XM_011526213.2:c.3909G>C | XP_011524515.1:p.Leu1303Phe | |
| XM_017026012.1:c.3999G>C | XP_016881501.1:p.Leu1333Phe | |
| XM_017026013.1:c.3909G>C | XP_016881502.1:p.Leu1303Phe | |
| XM_017026014.2:c.3909G>C | XP_016881503.1:p.Leu1303Phe | |
| XM_024451269.1:c.3909G>C | XP_024307037.1:p.Leu1303Phe | |
| NM_030632.3:c.4077G>C MANE Select | NP_085135.1:p.Leu1359Phe |