Canonical Allele Identifier: CA1481522778

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102778621T= , CM000666.2:g.102778621T=	GRCh38
NC_000004.11:g.103699778T= , CM000666.1:g.103699778T=	GRCh37

Transcript Alleles

HGVS	Amino-acid Change
NR_125932.1:n.713-187T=