Linked Data
gnomAD v3:
6-31357442-C-A
gnomAD v4:
6-31357442-C-A
MyVariant Identifiers:
chr6:g.31325219C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31357442C>A , CM000668.2:g.31357442C>A | GRCh38 |
| NC_000006.11:g.31325219C>A , CM000668.1:g.31325219C>A | GRCh37 |
| NC_000006.10:g.31433198C>A | NCBI36 |
| NG_023187.1:g.4771G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000474381.2:n.1339-149G>T | ||
| ENST00000481849.6:n.1339-149G>T | ||
| ENST00000497377.6:n.1339-149G>T | ||
| ENST00000696559.1:c.-135-149G>T | ENSP00000512717.1:n.-135-149G>T | |
| ENST00000696560.1:c.-135-149G>T | ENSP00000512718.1:n.-135-149G>T | |
| ENST00000696561.1:c.-135-149G>T | ENSP00000512719.1:n.-135-149G>T | |
| ENST00000696562.1:c.-135-149G>T | ENSP00000512720.1:n.-135-149G>T | |
| ENST00000603274.1:n.796C>A | ||
| XR_926692.1:n.165-149G>T |