Canonical Allele Identifier: CA586000477

Gene: CD274

Linked Data

• dbSNP Id: rs1298784551
• gnomAD v2: 9-5455718-C-G
• MyVariant Identifiers: chr9:g.5455718C>G (hg19) ; chr9:g.5455718C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.5455718C>G , CM000671.2:g.5455718C>G	GRCh38
NC_000009.11:g.5455718C>G , CM000671.1:g.5455718C>G	GRCh37
NC_000009.10:g.5445718C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381577.4:c.-14-382C>G MANE Select	ENSP00000370989.3:n.-14-382C>G
ENST00000381573.8:c.-14-382C>G	ENSP00000370985.4:n.-14-382C>G
ENST00000381577.3:c.-14-382C>G	ENSP00000370989.3:n.-14-382C>G
NM_001267706.1:c.-14-382C>G	NP_001254635.1:n.-14-382C>G
NM_001314029.1:c.-14-382C>G	NP_001300958.1:n.-14-382C>G
NM_014143.3:c.-14-382C>G	NP_054862.1:n.-14-382C>G
NR_052005.1:n.95-382C>G
XM_006716759.2:c.-14-382C>G	XP_006716822.1:n.-14-382C>G
NM_014143.4:c.-14-382C>G MANE Select	NP_054862.1:n.-14-382C>G
NM_001314029.2:c.-14-382C>G	NP_001300958.1:n.-14-382C>G
NR_052005.2:n.56-382C>G
NM_001267706.2:c.-14-382C>G	NP_001254635.1:n.-14-382C>G