Canonical Allele Identifier: CA1287750281

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.129276439C>T , CM000664.2:g.129276439C>T	GRCh38
NC_000002.11:g.130034012C>T , CM000664.1:g.130034012C>T	GRCh37
NC_000002.10:g.129750482C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923320.1:n.1133-12511C>T