Canonical Allele Identifier: CA2330336255

Gene:

Linked Data

• dbSNP Id: rs2011164508

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.28544609T>C , CM000681.2:g.28544609T>C	GRCh38
NC_000019.9:g.29035516T>C , CM000681.1:g.29035516T>C	GRCh37
NC_000019.8:g.33727356T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110759.1:n.657-77829A>G
XR_243979.1:n.110-51586A>G