Canonical Allele Identifier: CA188503744
Gene: CD274 HGNC NCBI

Linked Data

dbSNP Id: rs1005222575
gnomAD v3: 9-5455636-G-C
gnomAD v4: 9-5455636-G-C
MyVariant Identifiers: chr9:g.5455636G>C (hg19) chr9:g.5455636G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.5455636G>C , CM000671.2:g.5455636G>C GRCh38
NC_000009.11:g.5455636G>C , CM000671.1:g.5455636G>C GRCh37
NC_000009.10:g.5445636G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000381577.4:c.-14-464G>C MANE Select ENSP00000370989.3:n.-14-464G>C
ENST00000381573.8:c.-14-464G>C ENSP00000370985.4:n.-14-464G>C
ENST00000381577.3:c.-14-464G>C ENSP00000370989.3:n.-14-464G>C
NM_001267706.1:c.-14-464G>C NP_001254635.1:n.-14-464G>C
NM_001314029.1:c.-14-464G>C NP_001300958.1:n.-14-464G>C
NM_014143.3:c.-14-464G>C NP_054862.1:n.-14-464G>C
NR_052005.1:n.95-464G>C
XM_006716759.2:c.-14-464G>C XP_006716822.1:n.-14-464G>C
NM_014143.4:c.-14-464G>C MANE Select NP_054862.1:n.-14-464G>C
NM_001314029.2:c.-14-464G>C NP_001300958.1:n.-14-464G>C
NR_052005.2:n.56-464G>C
NM_001267706.2:c.-14-464G>C NP_001254635.1:n.-14-464G>C
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