Canonical Allele Identifier: CA306408443
Gene:

Linked Data

dbSNP Id: rs114177360

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.20217961A>C , CM000681.2:g.20217961A>C GRCh38
NC_000019.9:g.20328770A>C , CM000681.1:g.20328770A>C GRCh37
NC_000019.8:g.20189770A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_936388.1:n.619-645T>G
XR_936389.1:n.502-645T>G
XR_936390.1:n.511-645T>G
XR_936391.1:n.514-645T>G
XR_936392.1:n.514-645T>G
XR_936394.1:n.41-773A>C
XR_001754063.2:n.1506-645T>G
XR_001754064.2:n.138-645T>G
XR_001754066.1:n.3912-645T>G
XR_001754067.1:n.3912-645T>G
XR_001754068.1:n.3912-645T>G
XR_936394.2:n.41-773A>C
XR_936406.2:n.1411-645T>G