Canonical Allele Identifier: CA154890331

Gene:

Linked Data

• dbSNP Id: rs956781074
• MyVariant Identifiers: chr7:g.17997568A>G (hg19) ; chr7:g.17957945A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.17957945A>G , CM000669.2:g.17957945A>G	GRCh38
NC_000007.13:g.17997568A>G , CM000669.1:g.17997568A>G	GRCh37
NC_000007.12:g.17964093A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_927078.1:n.271-725A>G