Linked Data
dbSNP Id:
rs186928221
gnomAD v2:
6-31321700-C-G
gnomAD v3:
6-31353923-C-G
gnomAD v4:
6-31353923-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31353923C>G , CM000668.2:g.31353923C>G | GRCh38 |
| NC_000006.11:g.31321700C>G , CM000668.1:g.31321700C>G | GRCh37 |
| NC_000006.10:g.31429679C>G | NCBI36 |
| NG_023187.1:g.8290G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000474381.2:n.3514G>C | ||
| ENST00000481849.6:n.3474G>C | ||
| ENST00000497377.6:n.3381G>C | ||
| ENST00000696558.1:c.1536G>C | ENSP00000512716.1:n.1536G>C | |
| ENST00000696559.1:c.*378G>C | ENSP00000512717.1:n.*378G>C | |
| ENST00000696560.1:c.*378G>C | ENSP00000512718.1:n.*378G>C | |
| ENST00000696561.1:c.*378G>C | ENSP00000512719.1:n.*378G>C | |
| ENST00000696562.1:c.*378G>C | ENSP00000512720.1:n.*378G>C | |
| ENST00000412585.7:c.*378G>C MANE Select | ENSP00000399168.2:n.*378G>C | |
| ENST00000412585.6:c.*378G>C | ENSP00000399168.2:n.*378G>C | |
| ENST00000481849.5:n.702G>C | ||
| ENST00000497377.5:n.866G>C | ||
| NM_005514.6:c.*378G>C | NP_005505.2:n.*378G>C | |
| XM_011514556.1:c.*378G>C | XP_011512858.1:n.*378G>C | |
| XM_011514557.1:c.*378G>C | XP_011512859.1:n.*378G>C | |
| XR_926175.1:n.1906G>C | ||
| NM_005514.7:c.*378G>C | NP_005505.2:n.*378G>C | |
| NM_005514.8:c.*378G>C MANE Select | NP_005505.2:n.*378G>C |