Canonical Allele Identifier: CA200491727
Gene:

Linked Data

dbSNP Id: rs1007003481

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129576871T>C , CM000671.2:g.129576871T>C GRCh38
NC_000009.11:g.132339150T>C , CM000671.1:g.132339150T>C GRCh37
NC_000009.10:g.131378971T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930390.1:n.182+1273T>C