Canonical Allele Identifier: CA1648334931

Gene:

Linked Data

• dbSNP Id: rs2380220

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.95519536T>G , CM000668.2:g.95519536T>G	GRCh38
NC_000006.11:g.95967412T>G , CM000668.1:g.95967412T>G	GRCh37
NC_000006.10:g.96074133T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_942795.1:n.30A>C