Canonical Allele Identifier: CA1350284070
Gene:

Linked Data

dbSNP Id: rs1698204266

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.21207167G>T , CM000665.2:g.21207167G>T GRCh38
NC_000003.11:g.21248659G>T , CM000665.1:g.21248659G>T GRCh37
NC_000003.10:g.21223663G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940646.1:n.254-3831G>T
XR_940646.2:n.547-3831G>T