Canonical Allele Identifier: CA914308770
Gene:

Linked Data

dbSNP Id: rs1555721044

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.20218296G>C , CM000681.2:g.20218296G>C GRCh38
NC_000019.9:g.20329105G>C , CM000681.1:g.20329105G>C GRCh37
NC_000019.8:g.20190105G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_936388.1:n.619-980C>G
XR_936389.1:n.502-980C>G
XR_936390.1:n.511-980C>G
XR_936391.1:n.514-980C>G
XR_936392.1:n.514-980C>G
XR_936394.1:n.41-438G>C
XR_001754063.2:n.1506-980C>G
XR_001754064.2:n.138-980C>G
XR_001754066.1:n.3912-980C>G
XR_001754067.1:n.3912-980C>G
XR_001754068.1:n.3912-980C>G
XR_936394.2:n.41-438G>C
XR_936406.2:n.1411-980C>G