Canonical Allele Identifier: CA1769514552
Gene:

Linked Data

dbSNP Id: rs1799796390

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.20734953A>C , CM000670.2:g.20734953A>C GRCh38
NC_000008.10:g.20592464A>C , CM000670.1:g.20592464A>C GRCh37
NC_000008.9:g.20636744A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949569.3:n.72-55493A>C