Canonical Allele Identifier: CA2735724466

Gene:

Linked Data

• dbSNP Id: rs2145087528

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.28544810G>C , CM000681.2:g.28544810G>C	GRCh38
NC_000019.9:g.29035717G>C , CM000681.1:g.29035717G>C	GRCh37
NC_000019.8:g.33727557G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_110759.1:n.657-78030C>G
XR_243979.1:n.110-51787C>G