Canonical Allele Identifier:
CA448169025
Gene:
MyVariant.info:
GRCh37
chr6:g.2912277G>C
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.2912043G>C , CM000668.2:g.2912043G>C | GRCh38 |
| NC_000006.11:g.2912277G>C , CM000668.1:g.2912277G>C | GRCh37 |
| NC_000006.10:g.2857276G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000454998.1:n.71C>G |