Canonical Allele Identifier: CA2493232047
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.20485586C= , CM000664.2:g.20485586C= GRCh38
NC_000002.11:g.20685347C= , CM000664.1:g.20685347C= GRCh37
NC_000002.10:g.20548828C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_157978.1:n.530+3152G=