Canonical Allele Identifier: CA188512109

Gene: CD274

Linked Data

• dbSNP Id: rs1056422938
• MyVariant Identifiers: chr9:g.5468340G>A (hg19) ; chr9:g.5468340G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.5468340G>A , CM000671.2:g.5468340G>A	GRCh38
NC_000009.11:g.5468340G>A , CM000671.1:g.5468340G>A	GRCh37
NC_000009.10:g.5458340G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381577.4:c.*478G>A MANE Select	ENSP00000370989.3:n.*478G>A
ENST00000381573.8:c.*478G>A	ENSP00000370985.4:n.*478G>A
ENST00000381577.3:c.*478G>A	ENSP00000370989.3:n.*478G>A
NM_001267706.1:c.*478G>A	NP_001254635.1:n.*478G>A
NM_014143.3:c.*478G>A	NP_054862.1:n.*478G>A
NR_052005.1:n.1286G>A
NM_014143.4:c.*478G>A MANE Select	NP_054862.1:n.*478G>A
NR_052005.2:n.1247G>A
NM_001267706.2:c.*478G>A	NP_001254635.1:n.*478G>A