Canonical Allele Identifier: CA188503754
Gene: CD274 HGNC NCBI

Linked Data

dbSNP Id: rs1056122354
gnomAD v3: 9-5455665-T-C
gnomAD v4: 9-5455665-T-C
MyVariant Identifiers: chr9:g.5455665T>C (hg19) chr9:g.5455665T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.5455665T>C , CM000671.2:g.5455665T>C GRCh38
NC_000009.11:g.5455665T>C , CM000671.1:g.5455665T>C GRCh37
NC_000009.10:g.5445665T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000381577.4:c.-14-435T>C MANE Select ENSP00000370989.3:n.-14-435T>C
ENST00000381573.8:c.-14-435T>C ENSP00000370985.4:n.-14-435T>C
ENST00000381577.3:c.-14-435T>C ENSP00000370989.3:n.-14-435T>C
NM_001267706.1:c.-14-435T>C NP_001254635.1:n.-14-435T>C
NM_001314029.1:c.-14-435T>C NP_001300958.1:n.-14-435T>C
NM_014143.3:c.-14-435T>C NP_054862.1:n.-14-435T>C
NR_052005.1:n.95-435T>C
XM_006716759.2:c.-14-435T>C XP_006716822.1:n.-14-435T>C
NM_014143.4:c.-14-435T>C MANE Select NP_054862.1:n.-14-435T>C
NM_001314029.2:c.-14-435T>C NP_001300958.1:n.-14-435T>C
NR_052005.2:n.56-435T>C
NM_001267706.2:c.-14-435T>C NP_001254635.1:n.-14-435T>C
Search 100 bp 5'
Search 100 bp 3'