Canonical Allele Identifier: CA890857345

Gene:

Linked Data

• dbSNP Id: rs1459767848
• MyVariant Identifiers: chr1:g.168618785T>A (hg19) ; chr1:g.168649547T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.168649547T>A , CM000663.2:g.168649547T>A	GRCh38
NC_000001.10:g.168618785T>A , CM000663.1:g.168618785T>A	GRCh37
NC_000001.9:g.166885409T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_922259.1:n.201-8272A>T
XR_922259.2:n.332-8272A>T