Canonical Allele Identifier: CA185200429

Gene:

Linked Data

• dbSNP Id: rs760105902
• MyVariant Identifiers: chr8:g.123408320C>A (hg19) ; chr8:g.122396081C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.122396081C>A , CM000670.2:g.122396081C>A	GRCh38
NC_000008.10:g.123408320C>A , CM000670.1:g.123408320C>A	GRCh37
NC_000008.9:g.123477501C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_928599.1:n.152+3091G>T
XR_928599.3:n.152+3091G>T