Linked Data
gnomAD v3:
6-31354664-A-G
gnomAD v4:
6-31354664-A-G
MyVariant Identifiers:
chr6:g.31322441A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31354664A>G , CM000668.2:g.31354664A>G | GRCh38 |
| NC_000006.11:g.31322441A>G , CM000668.1:g.31322441A>G | GRCh37 |
| NC_000006.10:g.31430420A>G | NCBI36 |
| NG_023187.1:g.7549T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000474381.2:n.3061T>C | ||
| ENST00000481849.6:n.3021T>C | ||
| ENST00000497377.6:n.2928T>C | ||
| ENST00000640094.2:c.897T>C | ENSP00000491275.2:p.Gly299= | |
| ENST00000696558.1:c.1083T>C | ENSP00000512716.1:n.1083T>C | |
| ENST00000696559.1:c.1014T>C | ENSP00000512717.1:p.Gly338= | |
| ENST00000696560.1:c.1014T>C | ENSP00000512718.1:p.Gly338= | |
| ENST00000696561.1:c.1014T>C | ENSP00000512719.1:p.Gly338= | |
| ENST00000696562.1:c.1014T>C | ENSP00000512720.1:p.Gly338= | |
| ENST00000412585.7:c.1014T>C MANE Select | ENSP00000399168.2:p.Gly338= | |
| ENST00000640094.1:c.90T>C | ENSP00000491275.1:p.Gly30= | |
| ENST00000412585.6:c.1014T>C | ENSP00000399168.2:p.Gly338= | |
| ENST00000481849.5:n.143T>C | ||
| ENST00000497377.5:n.413T>C | ||
| NM_005514.6:c.1014T>C | NP_005505.2:p.Gly338= | |
| XM_011514556.1:c.1047T>C | XP_011512858.1:p.Gly349= | |
| XM_011514557.1:c.897T>C | XP_011512859.1:p.Gly299= | |
| XR_926175.1:n.1453T>C | ||
| NM_005514.7:c.1014T>C | NP_005505.2:p.Gly338= | |
| NM_005514.8:c.1014T>C MANE Select | NP_005505.2:p.Gly338= |