Canonical Allele Identifier: CA786695554
Gene:

Linked Data

dbSNP Id: rs1378413585

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578244C>A , CM000666.2:g.12578244C>A GRCh38
NC_000004.11:g.12579868C>A , CM000666.1:g.12579868C>A GRCh37
NC_000004.10:g.12188966C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31098G>T
XR_001741374.1:n.254+44411G>T
XR_925406.3:n.140+31098G>T