Canonical Allele Identifier: CA2193710615
Gene:

Linked Data

dbSNP Id: rs1895002680

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.87419477G>A , CM000677.2:g.87419477G>A GRCh38
NC_000015.9:g.87962708G>A , CM000677.1:g.87962708G>A GRCh37
NC_000015.8:g.85763712G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_932584.1:n.340-206C>T
XR_932585.1:n.340-206C>T
XR_001751647.1:n.617-206C>T
XR_932585.2:n.627-206C>T