Canonical Allele Identifier: CA1672979339

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151633784T= , CM000668.2:g.151633784T=	GRCh38
NC_000006.11:g.151954919T= , CM000668.1:g.151954919T=	GRCh37
NC_000006.10:g.151996612T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943115.1:n.2496+3802T=