Canonical Allele Identifier: CA1320446178

Gene:

Linked Data

• dbSNP Id: rs2077889186

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.200033236C>T , CM000664.2:g.200033236C>T	GRCh38
NC_000002.11:g.200897959C>T , CM000664.1:g.200897959C>T	GRCh37
NC_000002.10:g.200606204C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923778.1:n.178-22340G>A