Canonical Allele Identifier: CA1829889895
Gene: CD274 HGNC NCBI

Linked Data

dbSNP Id: rs1819291020
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.5455809A>G , CM000671.2:g.5455809A>G GRCh38
NC_000009.11:g.5455809A>G , CM000671.1:g.5455809A>G GRCh37
NC_000009.10:g.5445809A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000381577.4:c.-14-291A>G MANE Select ENSP00000370989.3:n.-14-291A>G
ENST00000381573.8:c.-14-291A>G ENSP00000370985.4:n.-14-291A>G
ENST00000381577.3:c.-14-291A>G ENSP00000370989.3:n.-14-291A>G
NM_001267706.1:c.-14-291A>G NP_001254635.1:n.-14-291A>G
NM_001314029.1:c.-14-291A>G NP_001300958.1:n.-14-291A>G
NM_014143.3:c.-14-291A>G NP_054862.1:n.-14-291A>G
NR_052005.1:n.95-291A>G
XM_006716759.2:c.-14-291A>G XP_006716822.1:n.-14-291A>G
NM_014143.4:c.-14-291A>G MANE Select NP_054862.1:n.-14-291A>G
NM_001314029.2:c.-14-291A>G NP_001300958.1:n.-14-291A>G
NR_052005.2:n.56-291A>G
NM_001267706.2:c.-14-291A>G NP_001254635.1:n.-14-291A>G
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