Canonical Allele Identifier: CA173695191

Gene:

Linked Data

• dbSNP Id: rs2122469
• MyVariant Identifiers: chr8:g.20626321G>T (hg19) ; chr8:g.20768810G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.20768810G>T , CM000670.2:g.20768810G>T	GRCh38
NC_000008.10:g.20626321G>T , CM000670.1:g.20626321G>T	GRCh37
NC_000008.9:g.20670601G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_949569.3:n.72-21636G>T