Canonical Allele Identifier: CA2689322436
Gene: CD274 HGNC NCBI

Linked Data

gnomAD v4: 9-5468278-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.5468278C>A , CM000671.2:g.5468278C>A GRCh38
NC_000009.11:g.5468278C>A , CM000671.1:g.5468278C>A GRCh37
NC_000009.10:g.5458278C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000381577.4:c.*416C>A MANE Select ENSP00000370989.3:n.*416C>A
ENST00000381573.8:c.*416C>A ENSP00000370985.4:n.*416C>A
ENST00000381577.3:c.*416C>A ENSP00000370989.3:n.*416C>A
NM_001267706.1:c.*416C>A NP_001254635.1:n.*416C>A
NM_014143.3:c.*416C>A NP_054862.1:n.*416C>A
NR_052005.1:n.1224C>A
NM_014143.4:c.*416C>A MANE Select NP_054862.1:n.*416C>A
NR_052005.2:n.1185C>A
NM_001267706.2:c.*416C>A NP_001254635.1:n.*416C>A
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