Canonical Allele Identifier: CA2689322423
Gene: CD274 HGNC NCBI

Linked Data

gnomAD v4: 9-5468267-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.5468267T>C , CM000671.2:g.5468267T>C GRCh38
NC_000009.11:g.5468267T>C , CM000671.1:g.5468267T>C GRCh37
NC_000009.10:g.5458267T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000381577.4:c.*405T>C MANE Select ENSP00000370989.3:n.*405T>C
ENST00000381573.8:c.*405T>C ENSP00000370985.4:n.*405T>C
ENST00000381577.3:c.*405T>C ENSP00000370989.3:n.*405T>C
NM_001267706.1:c.*405T>C NP_001254635.1:n.*405T>C
NM_014143.3:c.*405T>C NP_054862.1:n.*405T>C
NR_052005.1:n.1213T>C
NM_014143.4:c.*405T>C MANE Select NP_054862.1:n.*405T>C
NR_052005.2:n.1174T>C
NM_001267706.2:c.*405T>C NP_001254635.1:n.*405T>C
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