Canonical Allele Identifier: CA1120809551
Gene: CD274 HGNC NCBI

Linked Data

dbSNP Id: rs1819530068
gnomAD v3: 9-5468270-C-T
gnomAD v4: 9-5468270-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.5468270C>T , CM000671.2:g.5468270C>T GRCh38
NC_000009.11:g.5468270C>T , CM000671.1:g.5468270C>T GRCh37
NC_000009.10:g.5458270C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000381577.4:c.*408C>T MANE Select ENSP00000370989.3:n.*408C>T
ENST00000381573.8:c.*408C>T ENSP00000370985.4:n.*408C>T
ENST00000381577.3:c.*408C>T ENSP00000370989.3:n.*408C>T
NM_001267706.1:c.*408C>T NP_001254635.1:n.*408C>T
NM_014143.3:c.*408C>T NP_054862.1:n.*408C>T
NR_052005.1:n.1216C>T
NM_014143.4:c.*408C>T MANE Select NP_054862.1:n.*408C>T
NR_052005.2:n.1177C>T
NM_001267706.2:c.*408C>T NP_001254635.1:n.*408C>T
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