Canonical Allele Identifier: CA93117872

Gene:

Linked Data

• dbSNP Id: rs982888565
• MyVariant Identifiers: chr4:g.12579569A>G (hg19) ; chr4:g.12577945A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.12577945A>G , CM000666.2:g.12577945A>G	GRCh38
NC_000004.11:g.12579569A>G , CM000666.1:g.12579569A>G	GRCh37
NC_000004.10:g.12188667A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_925406.1:n.106+31397T>C
XR_001741374.1:n.254+44710T>C
XR_925406.3:n.140+31397T>C