Linked Data
dbSNP Id:
rs1330590202
gnomAD v2:
6-31324976-G-T
gnomAD v3:
6-31357199-G-T
gnomAD v4:
6-31357199-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31357199G>T , CM000668.2:g.31357199G>T | GRCh38 |
| NC_000006.11:g.31324976G>T , CM000668.1:g.31324976G>T | GRCh37 |
| NC_000006.10:g.31432955G>T | NCBI36 |
| NG_023187.1:g.5014C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000474381.2:n.1433C>A | ||
| ENST00000481849.6:n.1433C>A | ||
| ENST00000497377.6:n.1433C>A | ||
| ENST00000696559.1:c.-41C>A | ENSP00000512717.1:n.-41C>A | |
| ENST00000696560.1:c.-41C>A | ENSP00000512718.1:n.-41C>A | |
| ENST00000696561.1:c.-41C>A | ENSP00000512719.1:n.-41C>A | |
| ENST00000696562.1:c.-41C>A | ENSP00000512720.1:n.-41C>A | |
| ENST00000603274.1:n.553G>T | ||
| NM_005514.6:c.-41C>A | NP_005505.2:n.-41C>A | |
| NM_005514.7:c.-41C>A | NP_005505.2:n.-41C>A |