Canonical Allele Identifier: CA14888673
Gene:

Linked Data

dbSNP Id: rs1297265

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.15444732A>G , CM000683.2:g.15444732A>G GRCh38
NC_000021.8:g.16817051A>G , CM000683.1:g.16817051A>G GRCh37
NC_000021.7:g.15738922A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001754965.2:n.52T>C
XR_001754970.2:n.52T>C
XR_001754971.2:n.52T>C