Canonical Allele Identifier: CA2493232057
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.20485606A= , CM000664.2:g.20485606A= GRCh38
NC_000002.11:g.20685367A= , CM000664.1:g.20685367A= GRCh37
NC_000002.10:g.20548848A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_157978.1:n.530+3132T=