Linked Data
gnomAD v3:
6-31357159-C-A
gnomAD v4:
6-31357159-C-A
MyVariant Identifiers:
chr6:g.31324936C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31357159C>A , CM000668.2:g.31357159C>A | GRCh38 |
| NC_000006.11:g.31324936C>A , CM000668.1:g.31324936C>A | GRCh37 |
| NC_000006.10:g.31432915C>A | NCBI36 |
| NG_023187.1:g.5054G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000474381.2:n.1473G>T | ||
| ENST00000481849.6:n.1473G>T | ||
| ENST00000497377.6:n.1473G>T | ||
| ENST00000696559.1:c.-1G>T | ENSP00000512717.1:n.-1G>T | |
| ENST00000696560.1:c.-1G>T | ENSP00000512718.1:n.-1G>T | |
| ENST00000696561.1:c.-1G>T | ENSP00000512719.1:n.-1G>T | |
| ENST00000696562.1:c.-1G>T | ENSP00000512720.1:n.-1G>T | |
| ENST00000412585.7:c.-1G>T MANE Select | ENSP00000399168.2:n.-1G>T | |
| ENST00000412585.6:c.-1G>T | ENSP00000399168.2:n.-1G>T | |
| ENST00000434333.1:c.-96G>T | ENSP00000405931.1:n.-96G>T | |
| ENST00000498007.1:n.21G>T | ||
| ENST00000603274.1:n.513C>A | ||
| NM_005514.6:c.-1G>T | NP_005505.2:n.-1G>T | |
| XM_011514557.1:c.-1G>T | XP_011512859.1:n.-1G>T | |
| XR_926175.1:n.10G>T | ||
| NM_005514.7:c.-1G>T | NP_005505.2:n.-1G>T | |
| NM_005514.8:c.-1G>T MANE Select | NP_005505.2:n.-1G>T |