Canonical Allele Identifier: CA1880834385

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.129576847T= , CM000671.2:g.129576847T=	GRCh38
NC_000009.11:g.132339126T= , CM000671.1:g.132339126T=	GRCh37
NC_000009.10:g.131378947T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930390.1:n.182+1249T=