Canonical Allele Identifier: CA880474432
Gene:

Linked Data

dbSNP Id: rs1436713624
MyVariant Identifiers: chr19:g.20218338T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.20218338T>C , CM000681.2:g.20218338T>C GRCh38
NC_000019.9:g.20329147T>C , CM000681.1:g.20329147T>C GRCh37
NC_000019.8:g.20190147T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_936388.1:n.619-1022A>G
XR_936389.1:n.502-1022A>G
XR_936390.1:n.511-1022A>G
XR_936391.1:n.514-1022A>G
XR_936392.1:n.514-1022A>G
XR_936394.1:n.41-396T>C
XR_001754063.2:n.1506-1022A>G
XR_001754064.2:n.138-1022A>G
XR_001754066.1:n.3912-1022A>G
XR_001754067.1:n.3912-1022A>G
XR_001754068.1:n.3912-1022A>G
XR_936394.2:n.41-396T>C
XR_936406.2:n.1411-1022A>G