Canonical Allele Identifier: CA13378024
Gene:

Linked Data

dbSNP Id: rs3925584

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.30738788T>C , CM000673.2:g.30738788T>C GRCh38
NC_000011.9:g.30760335T>C , CM000673.1:g.30760335T>C GRCh37
NC_000011.8:g.30716911T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001748483.1:n.958-2627T>C
XR_242862.4:n.958-2627T>C