Canonical Allele Identifier: CA880474206
Gene:

Linked Data

dbSNP Id: rs1219362366
MyVariant Identifiers: chr19:g.20217936T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.20217936T>C , CM000681.2:g.20217936T>C GRCh38
NC_000019.9:g.20328745T>C , CM000681.1:g.20328745T>C GRCh37
NC_000019.8:g.20189745T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_936388.1:n.619-620A>G
XR_936389.1:n.502-620A>G
XR_936390.1:n.511-620A>G
XR_936391.1:n.514-620A>G
XR_936392.1:n.514-620A>G
XR_936394.1:n.41-798T>C
XR_001754063.2:n.1506-620A>G
XR_001754064.2:n.138-620A>G
XR_001754066.1:n.3912-620A>G
XR_001754067.1:n.3912-620A>G
XR_001754068.1:n.3912-620A>G
XR_936394.2:n.41-798T>C
XR_936406.2:n.1411-620A>G