Canonical Allele Identifier: CA1373744057
Gene:

Linked Data

dbSNP Id: rs1701575084

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.70577229G>A , CM000665.2:g.70577229G>A GRCh38
NC_000003.11:g.70626380G>A , CM000665.1:g.70626380G>A GRCh37
NC_000003.10:g.70709070G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940947.1:n.407-1276C>T
XR_001740559.1:n.367-1276C>T