Canonical Allele Identifier: CA127628855

Gene:

Linked Data

• dbSNP Id: rs189215657
• MyVariant Identifiers: chr5:g.128722574A>G (hg19) ; chr5:g.129386881A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.129386881A>G , CM000667.2:g.129386881A>G	GRCh38
NC_000005.9:g.128722574A>G , CM000667.1:g.128722574A>G	GRCh37
NC_000005.8:g.128750473A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_427770.2:n.163-1567A>G
XR_948774.1:n.235-5770A>G
XR_001742463.1:n.4089-1567A>G
XR_001742464.1:n.2019-5770A>G
XR_001742465.1:n.401-1567A>G
XR_427770.3:n.337-1567A>G