Canonical Allele Identifier: CA181599873

Gene:

Linked Data

• dbSNP Id: rs901685298
• MyVariant Identifiers: chr8:g.89993415C>T (hg19) ; chr8:g.88981186C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.88981186C>T , CM000670.2:g.88981186C>T	GRCh38
NC_000008.10:g.89993415C>T , CM000670.1:g.89993415C>T	GRCh37
NC_000008.9:g.90062531C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_002956667.1:n.179-99125G>A