Canonical Allele Identifier: CA191701691

Gene:

Linked Data

• dbSNP Id: rs776938782
• MyVariant Identifiers: chr9:g.25551291C>T (hg19) ; chr9:g.25551293C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.25551293C>T , CM000671.2:g.25551293C>T	GRCh38
NC_000009.11:g.25551291C>T , CM000671.1:g.25551291C>T	GRCh37
NC_000009.10:g.25541291C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_929525.1:n.50-721G>A
XR_929525.2:n.674-721G>A