Canonical Allele Identifier: CA2689322428
Gene: CD274 HGNC NCBI

Linked Data

gnomAD v4: 9-5468272-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.5468272G>A , CM000671.2:g.5468272G>A GRCh38
NC_000009.11:g.5468272G>A , CM000671.1:g.5468272G>A GRCh37
NC_000009.10:g.5458272G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000381577.4:c.*410G>A MANE Select ENSP00000370989.3:n.*410G>A
ENST00000381573.8:c.*410G>A ENSP00000370985.4:n.*410G>A
ENST00000381577.3:c.*410G>A ENSP00000370989.3:n.*410G>A
NM_001267706.1:c.*410G>A NP_001254635.1:n.*410G>A
NM_014143.3:c.*410G>A NP_054862.1:n.*410G>A
NR_052005.1:n.1218G>A
NM_014143.4:c.*410G>A MANE Select NP_054862.1:n.*410G>A
NR_052005.2:n.1179G>A
NM_001267706.2:c.*410G>A NP_001254635.1:n.*410G>A
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