Canonical Allele Identifier: CA188503805

Gene: CD274

Linked Data

• dbSNP Id: rs954417402
• MyVariant Identifiers: chr9:g.5455710C>T (hg19) ; chr9:g.5455710C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.5455710C>T , CM000671.2:g.5455710C>T	GRCh38
NC_000009.11:g.5455710C>T , CM000671.1:g.5455710C>T	GRCh37
NC_000009.10:g.5445710C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381577.4:c.-14-390C>T MANE Select	ENSP00000370989.3:n.-14-390C>T
ENST00000381573.8:c.-14-390C>T	ENSP00000370985.4:n.-14-390C>T
ENST00000381577.3:c.-14-390C>T	ENSP00000370989.3:n.-14-390C>T
NM_001267706.1:c.-14-390C>T	NP_001254635.1:n.-14-390C>T
NM_001314029.1:c.-14-390C>T	NP_001300958.1:n.-14-390C>T
NM_014143.3:c.-14-390C>T	NP_054862.1:n.-14-390C>T
NR_052005.1:n.95-390C>T
XM_006716759.2:c.-14-390C>T	XP_006716822.1:n.-14-390C>T
NM_014143.4:c.-14-390C>T MANE Select	NP_054862.1:n.-14-390C>T
NM_001314029.2:c.-14-390C>T	NP_001300958.1:n.-14-390C>T
NR_052005.2:n.56-390C>T
NM_001267706.2:c.-14-390C>T	NP_001254635.1:n.-14-390C>T