Canonical Allele Identifier: CA14658029
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs1654260

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.20218302G>A , CM000681.2:g.20218302G>A GRCh38
NC_000019.9:g.20329111G>A , CM000681.1:g.20329111G>A GRCh37
NC_000019.8:g.20190111G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_936388.1:n.619-986C>T
XR_936389.1:n.502-986C>T
XR_936390.1:n.511-986C>T
XR_936391.1:n.514-986C>T
XR_936392.1:n.514-986C>T
XR_936394.1:n.41-432G>A
XR_001754063.2:n.1506-986C>T
XR_001754064.2:n.138-986C>T
XR_001754066.1:n.3912-986C>T
XR_001754067.1:n.3912-986C>T
XR_001754068.1:n.3912-986C>T
XR_936394.2:n.41-432G>A
XR_936406.2:n.1411-986C>T