Canonical Allele Identifier: CA14876182
Gene:

Linked Data

dbSNP Id: rs2823256

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.15412387G>A , CM000683.2:g.15412387G>A GRCh38
NC_000021.8:g.16784706G>A , CM000683.1:g.16784706G>A GRCh37
NC_000021.7:g.15706577G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_937593.1:n.553-6623C>T
XR_001754965.2:n.469-11838C>T
XR_001754970.2:n.469-11838C>T
XR_001754971.2:n.469-16890C>T