Canonical Allele Identifier: CA652102553

Gene:

Linked Data

• dbSNP Id: rs933180899
• COSMIC: COSN15345564
• MyVariant Identifiers: chr8:g.33665865G>T (hg19) ; chr8:g.33808347G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.33808347G>T , CM000670.2:g.33808347G>T	GRCh38
NC_000008.10:g.33665865G>T , CM000670.1:g.33665865G>T	GRCh37
NC_000008.9:g.33785407G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_949659.1:n.240+11911G>T
XR_002956701.1:n.240+11911G>T