Canonical Allele Identifier: CA880474409
Gene:

Linked Data

dbSNP Id: rs1314677846
MyVariant Identifiers: chr19:g.20218274G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.20218274G>A , CM000681.2:g.20218274G>A GRCh38
NC_000019.9:g.20329083G>A , CM000681.1:g.20329083G>A GRCh37
NC_000019.8:g.20190083G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_936388.1:n.619-958C>T
XR_936389.1:n.502-958C>T
XR_936390.1:n.511-958C>T
XR_936391.1:n.514-958C>T
XR_936392.1:n.514-958C>T
XR_936394.1:n.41-460G>A
XR_001754063.2:n.1506-958C>T
XR_001754064.2:n.138-958C>T
XR_001754066.1:n.3912-958C>T
XR_001754067.1:n.3912-958C>T
XR_001754068.1:n.3912-958C>T
XR_936394.2:n.41-460G>A
XR_936406.2:n.1411-958C>T