Linked Data
dbSNP Id:
rs368844792
ExAC:
16:3779803 G / A
gnomAD v2:
16-3779803-G-A
gnomAD v4:
16-3729802-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.3729802G>A , CM000678.2:g.3729802G>A | GRCh38 |
| NC_000016.9:g.3779803G>A , CM000678.1:g.3779803G>A | GRCh37 |
| NC_000016.8:g.3719804G>A | NCBI36 |
| NG_009873.1:g.155319C>T | |
| NG_009873.2:g.155912C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262367.10:c.5245C>T MANE Select | ENSP00000262367.5:p.Leu1749= | |
| ENST00000262367.9:c.5245C>T | ENSP00000262367.5:p.Leu1749= | |
| ENST00000382070.7:c.5131C>T | ENSP00000371502.3:p.Leu1711= | |
| NM_001079846.1:c.5131C>T | NP_001073315.1:p.Leu1711= | |
| NM_004380.2:c.5245C>T | NP_004371.2:p.Leu1749= | |
| XM_005255124.3:c.5200C>T | XP_005255181.1:p.Leu1734= | |
| XM_005255125.3:c.4828C>T | XP_005255182.1:p.Leu1610= | |
| XM_006720848.2:c.4984C>T | XP_006720911.1:p.Leu1662= | |
| XM_011522380.1:c.5191C>T | XP_011520682.1:p.Leu1731= | |
| XM_011522381.1:c.4492C>T | XP_011520683.1:p.Leu1498= | |
| XM_005255124.4:c.5200C>T | XP_005255181.1:p.Leu1734= | |
| XM_005255125.4:c.4828C>T | XP_005255182.1:p.Leu1610= | |
| XM_006720848.3:c.4984C>T | XP_006720911.1:p.Leu1662= | |
| XM_011522381.2:c.4492C>T | XP_011520683.1:p.Leu1498= | |
| XM_017022944.1:c.5239C>T | XP_016878433.1:p.Leu1747= | |
| NM_004380.3:c.5245C>T MANE Select | NP_004371.2:p.Leu1749= |