Canonical Allele Identifier: CA1237301125
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.9119469T= , CM000664.2:g.9119469T= GRCh38
NC_000002.11:g.9259598T= , CM000664.1:g.9259598T= GRCh37
NC_000002.10:g.9177049T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922770.1:n.831+795A=