Canonical Allele Identifier: CA994367861
Gene:

Linked Data

dbSNP Id: rs2090129405

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.20218347T>C , CM000681.2:g.20218347T>C GRCh38
NC_000019.9:g.20329156T>C , CM000681.1:g.20329156T>C GRCh37
NC_000019.8:g.20190156T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_936388.1:n.619-1031A>G
XR_936389.1:n.502-1031A>G
XR_936390.1:n.511-1031A>G
XR_936391.1:n.514-1031A>G
XR_936392.1:n.514-1031A>G
XR_936394.1:n.41-387T>C
XR_001754063.2:n.1506-1031A>G
XR_001754064.2:n.138-1031A>G
XR_001754066.1:n.3912-1031A>G
XR_001754067.1:n.3912-1031A>G
XR_001754068.1:n.3912-1031A>G
XR_936394.2:n.41-387T>C
XR_936406.2:n.1411-1031A>G