Canonical Allele Identifier: CA707588518

Gene:

Linked Data

• dbSNP Id: rs1489844710
• MyVariant Identifiers: chr14:g.62968319A>G (hg19) ; chr14:g.62501601A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.62501601A>G , CM000676.2:g.62501601A>G	GRCh38
NC_000014.8:g.62968319A>G , CM000676.1:g.62968319A>G	GRCh37
NC_000014.7:g.62038072A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_943932.1:n.116-2440A>G
XR_943932.2:n.103-2440A>G