Canonical Allele Identifier: CA306408553
Gene:

Linked Data

dbSNP Id: rs973833044
MyVariant Identifiers: chr19:g.20218286G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.20218286G>A , CM000681.2:g.20218286G>A GRCh38
NC_000019.9:g.20329095G>A , CM000681.1:g.20329095G>A GRCh37
NC_000019.8:g.20190095G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_936388.1:n.619-970C>T
XR_936389.1:n.502-970C>T
XR_936390.1:n.511-970C>T
XR_936391.1:n.514-970C>T
XR_936392.1:n.514-970C>T
XR_936394.1:n.41-448G>A
XR_001754063.2:n.1506-970C>T
XR_001754064.2:n.138-970C>T
XR_001754066.1:n.3912-970C>T
XR_001754067.1:n.3912-970C>T
XR_001754068.1:n.3912-970C>T
XR_936394.2:n.41-448G>A
XR_936406.2:n.1411-970C>T