Canonical Allele Identifier: CA185690306

Gene:

Linked Data

• dbSNP Id: rs1054873565
• MyVariant Identifiers: chr8:g.128024846G>T (hg19) ; chr8:g.127012601G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127012601G>T , CM000670.2:g.127012601G>T	GRCh38
NC_000008.10:g.128024846G>T , CM000670.1:g.128024846G>T	GRCh37
NC_000008.9:g.128094028G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001746076.2:n.1364+5983G>T