Canonical Allele Identifier: CA1261549182

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74712049T= , CM000664.2:g.74712049T=	GRCh38
NC_000002.11:g.74939176T= , CM000664.1:g.74939176T=	GRCh37
NC_000002.10:g.74792684T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_427047.4:n.362T=