MyVariant.info:
GRCh37
chr7:g.105926331C>G
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.106285885C>G , CM000669.2:g.106285885C>G | GRCh38 |
| NC_000007.13:g.105926331C>G , CM000669.1:g.105926331C>G | GRCh37 |
| NC_000007.12:g.105713567C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000424768.2:c.-442G>C | ENSP00000390591.2:n.-442G>C | |
| ENST00000681255.1:c.-392G>C | ENSP00000506129.1:n.-392G>C | |
| ENST00000424768.1:c.-442G>C | ENSP00000390591.1:n.-442G>C |