Canonical Allele Identifier: CA1320446090

Gene:

Linked Data

• dbSNP Id: rs2077888534

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.200033071G>T , CM000664.2:g.200033071G>T	GRCh38
NC_000002.11:g.200897794G>T , CM000664.1:g.200897794G>T	GRCh37
NC_000002.10:g.200606039G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923778.1:n.178-22175C>A