Linked Data
gnomAD v3:
6-31357037-C-T
gnomAD v4:
6-31357037-C-T
MyVariant Identifiers:
chr6:g.31324814C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31357037C>T , CM000668.2:g.31357037C>T | GRCh38 |
| NC_000006.11:g.31324814C>T , CM000668.1:g.31324814C>T | GRCh37 |
| NC_000006.10:g.31432793C>T | NCBI36 |
| NG_023187.1:g.5176G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000474381.2:n.1546+49G>A | ||
| ENST00000481849.6:n.1546+49G>A | ||
| ENST00000497377.6:n.1546+49G>A | ||
| ENST00000640094.2:c.73+49G>A | ENSP00000491275.2:n.73+49G>A | |
| ENST00000696558.1:c.73+49G>A | ENSP00000512716.1:n.73+49G>A | |
| ENST00000696559.1:c.73+49G>A | ENSP00000512717.1:n.73+49G>A | |
| ENST00000696560.1:c.73+49G>A | ENSP00000512718.1:n.73+49G>A | |
| ENST00000696561.1:c.73+49G>A | ENSP00000512719.1:n.73+49G>A | |
| ENST00000696562.1:c.73+49G>A | ENSP00000512720.1:n.73+49G>A | |
| ENST00000412585.7:c.73+49G>A MANE Select | ENSP00000399168.2:n.73+49G>A | |
| ENST00000412585.6:c.73+49G>A | ENSP00000399168.2:n.73+49G>A | |
| ENST00000434333.1:c.27G>A | ENSP00000405931.1:p.Gly9= | |
| ENST00000498007.1:n.94+49G>A | ||
| ENST00000603274.1:n.391C>T | ||
| NM_005514.6:c.73+49G>A | NP_005505.2:n.73+49G>A | |
| XM_011514556.1:c.27G>A | XP_011512858.1:p.Gly9= | |
| XM_011514557.1:c.73+49G>A | XP_011512859.1:n.73+49G>A | |
| XR_926175.1:n.83+49G>A | ||
| NM_005514.7:c.73+49G>A | NP_005505.2:n.73+49G>A | |
| NM_005514.8:c.73+49G>A MANE Select | NP_005505.2:n.73+49G>A |