Linked Data
dbSNP Id:
rs767700153
ExAC:
6:139694340 G / A
gnomAD v2:
6-139694340-G-A
gnomAD v4:
6-139373203-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.139373203G>A , CM000668.2:g.139373203G>A | GRCh38 |
| NC_000006.11:g.139694340G>A , CM000668.1:g.139694340G>A | GRCh37 |
| NC_000006.10:g.139736033G>A | NCBI36 |
| NG_016169.1:g.6446C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367651.4:c.742C>T MANE Select | ENSP00000356623.2:p.Leu248= | |
| ENST00000367651.3:c.742C>T | ENSP00000356623.2:p.Leu248= | |
| ENST00000536159.2:c.742C>T | ENSP00000442831.1:p.Leu248= | |
| ENST00000537332.2:c.757C>T | ENSP00000444198.2:p.Leu253= | |
| ENST00000618718.1:c.571C>T | ENSP00000479918.1:p.Leu191= | |
| NM_001168388.2:c.742C>T | NP_001161860.1:p.Leu248= | |
| NM_001168389.2:c.757C>T | NP_001161861.2:p.Leu253= | |
| NM_006079.4:c.742C>T | NP_006070.2:p.Leu248= | |
| NM_006079.5:c.742C>T MANE Select | NP_006070.2:p.Leu248= | |
| NM_001168388.3:c.742C>T | NP_001161860.1:p.Leu248= | |
| NM_001168389.3:c.757C>T | NP_001161861.2:p.Leu253= |