Canonical Allele Identifier: CA855468172

Gene:

Linked Data

• dbSNP Id: rs1266431269
• MyVariant Identifiers: chr8:g.78325926C>T (hg19) ; chr8:g.77413690C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.77413690C>T , CM000670.2:g.77413690C>T	GRCh38
NC_000008.10:g.78325926C>T , CM000670.1:g.78325926C>T	GRCh37
NC_000008.9:g.78488481C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_929071.1:n.231-4988C>T
XR_001745963.1:n.191-4988C>T