Canonical Allele Identifier: CA154393480

Gene:

Linked Data

• dbSNP Id: rs952222079
• MyVariant Identifiers: chr7:g.13440269A>C (hg19) ; chr7:g.13400644A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.13400644A>C , CM000669.2:g.13400644A>C	GRCh38
NC_000007.13:g.13440269A>C , CM000669.1:g.13440269A>C	GRCh37
NC_000007.12:g.13406794A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001745097.1:n.147+90321A>C