Canonical Allele Identifier: CA1320446224

Gene:

Linked Data

• dbSNP Id: rs2077889545

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.200033313T>G , CM000664.2:g.200033313T>G	GRCh38
NC_000002.11:g.200898036T>G , CM000664.1:g.200898036T>G	GRCh37
NC_000002.10:g.200606281T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_923778.1:n.178-22417A>C