Canonical Allele Identifier: CA2327233065
Gene:

Linked Data

dbSNP Id: rs2090126674

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.20217980C>T , CM000681.2:g.20217980C>T GRCh38
NC_000019.9:g.20328789C>T , CM000681.1:g.20328789C>T GRCh37
NC_000019.8:g.20189789C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_936388.1:n.619-664G>A
XR_936389.1:n.502-664G>A
XR_936390.1:n.511-664G>A
XR_936391.1:n.514-664G>A
XR_936392.1:n.514-664G>A
XR_936394.1:n.41-754C>T
XR_001754063.2:n.1506-664G>A
XR_001754064.2:n.138-664G>A
XR_001754066.1:n.3912-664G>A
XR_001754067.1:n.3912-664G>A
XR_001754068.1:n.3912-664G>A
XR_936394.2:n.41-754C>T
XR_936406.2:n.1411-664G>A