Canonical Allele Identifier: CA154409001

Gene:

Linked Data

• dbSNP Id: rs1026993654
• MyVariant Identifiers: chr7:g.13553760A>G (hg19) ; chr7:g.13514135A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.13514135A>G , CM000669.2:g.13514135A>G	GRCh38
NC_000007.13:g.13553760A>G , CM000669.1:g.13553760A>G	GRCh37
NC_000007.12:g.13520285A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001745097.1:n.148-188181A>G