Canonical Allele Identifier: CA590667416
Gene:

Linked Data

dbSNP Id: rs1300074291

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129576801T>G , CM000671.2:g.129576801T>G GRCh38
NC_000009.11:g.132339080T>G , CM000671.1:g.132339080T>G GRCh37
NC_000009.10:g.131378901T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930390.1:n.182+1203T>G