Canonical Allele Identifier: CA860367893

Gene:

Linked Data

• dbSNP Id: rs1221114319
• MyVariant Identifiers: chr9:g.132339124T>C (hg19) ; chr9:g.129576845T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.129576845T>C , CM000671.2:g.129576845T>C	GRCh38
NC_000009.11:g.132339124T>C , CM000671.1:g.132339124T>C	GRCh37
NC_000009.10:g.131378945T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_930390.1:n.182+1247T>C