Linked Data
gnomAD v3:
6-31357177-T-G
gnomAD v4:
6-31357177-T-G
MyVariant Identifiers:
chr6:g.31324954T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31357177T>G , CM000668.2:g.31357177T>G | GRCh38 |
| NC_000006.11:g.31324954T>G , CM000668.1:g.31324954T>G | GRCh37 |
| NC_000006.10:g.31432933T>G | NCBI36 |
| NG_023187.1:g.5036A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000474381.2:n.1455A>C | ||
| ENST00000481849.6:n.1455A>C | ||
| ENST00000497377.6:n.1455A>C | ||
| ENST00000696559.1:c.-19A>C | ENSP00000512717.1:n.-19A>C | |
| ENST00000696560.1:c.-19A>C | ENSP00000512718.1:n.-19A>C | |
| ENST00000696561.1:c.-19A>C | ENSP00000512719.1:n.-19A>C | |
| ENST00000696562.1:c.-19A>C | ENSP00000512720.1:n.-19A>C | |
| ENST00000412585.7:c.-19A>C MANE Select | ENSP00000399168.2:n.-19A>C | |
| ENST00000412585.6:c.-19A>C | ENSP00000399168.2:n.-19A>C | |
| ENST00000434333.1:c.-114A>C | ENSP00000405931.1:n.-114A>C | |
| ENST00000498007.1:n.3A>C | ||
| ENST00000603274.1:n.531T>G | ||
| NM_005514.6:c.-19A>C | NP_005505.2:n.-19A>C | |
| NM_005514.7:c.-19A>C | NP_005505.2:n.-19A>C | |
| NM_005514.8:c.-19A>C MANE Select | NP_005505.2:n.-19A>C |