Canonical Allele Identifier:
CA442024389
Gene:
MyVariant.info:
GRCh37
chr4:g.165908721A>C
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.164987569A>C , CM000666.2:g.164987569A>C | GRCh38 |
| NC_000004.11:g.165908721A>C , CM000666.1:g.165908721A>C | GRCh37 |
| NC_000004.10:g.166128171A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000510050.1:n.305A>C |