Canonical Allele Identifier: CA93117908

Gene:

Linked Data

• dbSNP Id: rs990139855
• MyVariant Identifiers: chr4:g.12579788T>C (hg19) ; chr4:g.12578164T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.12578164T>C , CM000666.2:g.12578164T>C	GRCh38
NC_000004.11:g.12579788T>C , CM000666.1:g.12579788T>C	GRCh37
NC_000004.10:g.12188886T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_925406.1:n.106+31178A>G
XR_001741374.1:n.254+44491A>G
XR_925406.3:n.140+31178A>G