Canonical Allele Identifier: CA856948414

Gene:

Linked Data

• dbSNP Id: rs1193922845
• MyVariant Identifiers: chr8:g.9183262C>T (hg19) ; chr8:g.9325752C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.9325752C>T , CM000670.2:g.9325752C>T	GRCh38
NC_000008.10:g.9183262C>T , CM000670.1:g.9183262C>T	GRCh37
NC_000008.9:g.9220672C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_040039.1:n.364-150C>T