Canonical Allele Identifier: CA1620048538

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33518955G= , CM000668.2:g.33518955G=	GRCh38
NC_000006.11:g.33486732G= , CM000668.1:g.33486732G=	GRCh37
NC_000006.10:g.33594710G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001743876.1:n.144+410C=