Canonical Allele Identifier: CA175153968

Gene:

Linked Data

• dbSNP Id: rs541417608
• MyVariant Identifiers: chr8:g.33665724C>T (hg19) ; chr8:g.33808206C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.33808206C>T , CM000670.2:g.33808206C>T	GRCh38
NC_000008.10:g.33665724C>T , CM000670.1:g.33665724C>T	GRCh37
NC_000008.9:g.33785266C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_949659.1:n.240+11770C>T
XR_002956701.1:n.240+11770C>T