Canonical Allele Identifier: CA1332325195
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.226156030C= , CM000664.2:g.226156030C= GRCh38
NC_000002.11:g.227020746C= , CM000664.1:g.227020746C= GRCh37
NC_000002.10:g.226728990C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_046102.1:n.293-8358C=