Canonical Allele Identifier: CA833583510

Gene:

Linked Data

• dbSNP Id: rs1379079347
• MyVariant Identifiers: chr7:g.13440306A>T (hg19) ; chr7:g.13400681A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.13400681A>T , CM000669.2:g.13400681A>T	GRCh38
NC_000007.13:g.13440306A>T , CM000669.1:g.13440306A>T	GRCh37
NC_000007.12:g.13406831A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001745097.1:n.147+90358A>T