Canonical Allele Identifier: CA1338060475

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238295120T= , CM000664.2:g.238295120T=	GRCh38
NC_000002.11:g.239203761T= , CM000664.1:g.239203761T=	GRCh37
NC_000002.10:g.238868500T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_002959458.1:n.103-3257T=