Linked Data
gnomAD v3:
6-31356279-G-T
gnomAD v4:
6-31356279-G-T
MyVariant Identifiers:
chr6:g.31324056G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31356279G>T , CM000668.2:g.31356279G>T | GRCh38 |
| NC_000006.11:g.31324056G>T , CM000668.1:g.31324056G>T | GRCh37 |
| NC_000006.10:g.31432035G>T | NCBI36 |
| NG_023187.1:g.5934C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000474381.2:n.1980C>A | ||
| ENST00000481849.6:n.1980C>A | ||
| ENST00000497377.6:n.1980C>A | ||
| ENST00000640094.2:c.507C>A | ENSP00000491275.2:p.Arg169= | |
| ENST00000696558.1:c.507C>A | ENSP00000512716.1:p.Arg169= | |
| ENST00000696559.1:c.507C>A | ENSP00000512717.1:p.Arg169= | |
| ENST00000696560.1:c.507C>A | ENSP00000512718.1:p.Arg169= | |
| ENST00000696561.1:c.507C>A | ENSP00000512719.1:p.Arg169= | |
| ENST00000696562.1:c.507C>A | ENSP00000512720.1:p.Arg169= | |
| ENST00000412585.7:c.507C>A MANE Select | ENSP00000399168.2:p.Arg169= | |
| ENST00000412585.6:c.507C>A | ENSP00000399168.2:p.Arg169= | |
| ENST00000434333.1:c.540C>A | ENSP00000405931.1:p.Arg180= | |
| ENST00000474381.1:n.382C>A | ||
| ENST00000498007.1:n.773C>A | ||
| NM_005514.6:c.507C>A | NP_005505.2:p.Arg169= | |
| XM_011514556.1:c.540C>A | XP_011512858.1:p.Arg180= | |
| XM_011514557.1:c.507C>A | XP_011512859.1:p.Arg169= | |
| XR_926175.1:n.517C>A | ||
| NM_005514.7:c.507C>A | NP_005505.2:p.Arg169= | |
| NM_005514.8:c.507C>A MANE Select | NP_005505.2:p.Arg169= |