Canonical Allele Identifier: CA372837377

Gene: CD274

Linked Data

• dbSNP Id: rs17718883
• MyVariant Identifiers: chr9:g.5462876C>T (hg19) ; chr9:g.5462876C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.5462876C>T , CM000671.2:g.5462876C>T	GRCh38
NC_000009.11:g.5462876C>T , CM000671.1:g.5462876C>T	GRCh37
NC_000009.10:g.5452876C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000381577.4:c.437C>T MANE Select	ENSP00000370989.3:p.Pro146Leu
ENST00000381573.8:c.95C>T	ENSP00000370985.4:p.Pro32Leu
ENST00000381577.3:c.437C>T	ENSP00000370989.3:p.Pro146Leu
ENST00000474218.1:n.80C>T
ENST00000498261.1:n.437C>T
NM_001267706.1:c.95C>T	NP_001254635.1:p.Pro32Leu
NM_001314029.1:c.437C>T	NP_001300958.1:p.Pro146Leu
NM_014143.3:c.437C>T	NP_054862.1:p.Pro146Leu
NR_052005.1:n.545C>T
XM_006716759.2:c.437C>T	XP_006716822.1:p.Pro146Leu
NM_014143.4:c.437C>T MANE Select	NP_054862.1:p.Pro146Leu
NM_001314029.2:c.437C>T	NP_001300958.1:p.Pro146Leu
NR_052005.2:n.506C>T
NM_001267706.2:c.95C>T	NP_001254635.1:p.Pro32Leu