Canonical Allele Identifier: CA1120803422

Gene: CD274

Linked Data

• dbSNP Id: rs1819289232
• gnomAD v3: 9-5455706-A-T
• gnomAD v4: 9-5455706-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.5455706A>T , CM000671.2:g.5455706A>T	GRCh38
NC_000009.11:g.5455706A>T , CM000671.1:g.5455706A>T	GRCh37
NC_000009.10:g.5445706A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381577.4:c.-14-394A>T MANE Select	ENSP00000370989.3:n.-14-394A>T
ENST00000381573.8:c.-14-394A>T	ENSP00000370985.4:n.-14-394A>T
ENST00000381577.3:c.-14-394A>T	ENSP00000370989.3:n.-14-394A>T
NM_001267706.1:c.-14-394A>T	NP_001254635.1:n.-14-394A>T
NM_001314029.1:c.-14-394A>T	NP_001300958.1:n.-14-394A>T
NM_014143.3:c.-14-394A>T	NP_054862.1:n.-14-394A>T
NR_052005.1:n.95-394A>T
XM_006716759.2:c.-14-394A>T	XP_006716822.1:n.-14-394A>T
NM_014143.4:c.-14-394A>T MANE Select	NP_054862.1:n.-14-394A>T
NM_001314029.2:c.-14-394A>T	NP_001300958.1:n.-14-394A>T
NR_052005.2:n.56-394A>T
NM_001267706.2:c.-14-394A>T	NP_001254635.1:n.-14-394A>T