Linked Data
dbSNP Id:
rs1131446
gnomAD v3:
6-31355339-C-G
gnomAD v4:
6-31355339-C-G
MyVariant Identifiers:
chr6:g.31323116C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31355339C>G , CM000668.2:g.31355339C>G | GRCh38 |
| NC_000006.11:g.31323116C>G , CM000668.1:g.31323116C>G | GRCh37 |
| NC_000006.10:g.31431095C>G | NCBI36 |
| NG_023187.1:g.6874G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000474381.2:n.2920G>C | ||
| ENST00000481849.6:n.2346G>C | ||
| ENST00000497377.6:n.2346G>C | ||
| ENST00000640094.2:c.873G>C | ENSP00000491275.2:p.Pro291= | |
| ENST00000696558.1:c.942G>C | ENSP00000512716.1:n.942G>C | |
| ENST00000696559.1:c.873G>C | ENSP00000512717.1:p.Pro291= | |
| ENST00000696560.1:c.873G>C | ENSP00000512718.1:p.Pro291= | |
| ENST00000696561.1:c.873G>C | ENSP00000512719.1:p.Pro291= | |
| ENST00000696562.1:c.873G>C | ENSP00000512720.1:p.Pro291= | |
| ENST00000412585.7:c.873G>C MANE Select | ENSP00000399168.2:p.Pro291= | |
| ENST00000640094.1:c.66G>C | ENSP00000491275.1:p.Pro22= | |
| ENST00000412585.6:c.873G>C | ENSP00000399168.2:p.Pro291= | |
| ENST00000463574.1:n.464G>C | ||
| NM_005514.6:c.873G>C | NP_005505.2:p.Pro291= | |
| XM_011514556.1:c.906G>C | XP_011512858.1:p.Pro302= | |
| XM_011514557.1:c.873G>C | XP_011512859.1:p.Pro291= | |
| XR_926175.1:n.1312G>C | ||
| NM_005514.7:c.873G>C | NP_005505.2:p.Pro291= | |
| NM_005514.8:c.873G>C MANE Select | NP_005505.2:p.Pro291= |