Canonical Allele Identifier: CA188512031

Gene: CD274

Linked Data

• dbSNP Id: rs572112954
• gnomAD v3: 9-5468266-A-C
• gnomAD v4: 9-5468266-A-C
• MyVariant Identifiers: chr9:g.5468266A>C (hg19) ; chr9:g.5468266A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.5468266A>C , CM000671.2:g.5468266A>C	GRCh38
NC_000009.11:g.5468266A>C , CM000671.1:g.5468266A>C	GRCh37
NC_000009.10:g.5458266A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000381577.4:c.*404A>C MANE Select	ENSP00000370989.3:n.*404A>C
ENST00000381573.8:c.*404A>C	ENSP00000370985.4:n.*404A>C
ENST00000381577.3:c.*404A>C	ENSP00000370989.3:n.*404A>C
NM_001267706.1:c.*404A>C	NP_001254635.1:n.*404A>C
NM_014143.3:c.*404A>C	NP_054862.1:n.*404A>C
NR_052005.1:n.1212A>C
NM_014143.4:c.*404A>C MANE Select	NP_054862.1:n.*404A>C
NR_052005.2:n.1173A>C
NM_001267706.2:c.*404A>C	NP_001254635.1:n.*404A>C