Canonical Allele Identifier: CA763553027

Gene: CTLA4

Linked Data

• dbSNP Id: rs1250366178
• MyVariant Identifiers: chr2:g.204732576C>T (hg19) ; chr2:g.203867853C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203867853C>T , CM000664.2:g.203867853C>T	GRCh38
NC_000002.11:g.204732576C>T , CM000664.1:g.204732576C>T	GRCh37
NC_000002.10:g.204440821C>T	NCBI36
NG_011502.1:g.5068C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696049.1:c.-90C>T	ENSP00000512353.1:n.-90C>T
ENST00000696479.1:c.48-65C>T	ENSP00000512655.1:n.48-65C>T
ENST00000648405.2:c.-90C>T MANE Select	ENSP00000497102.1:n.-90C>T
ENST00000302823.7:c.-90C>T	ENSP00000303939.3:n.-90C>T
NM_001037631.2:c.-90C>T	NP_001032720.1:n.-90C>T
NM_005214.4:c.-90C>T	NP_005205.2:n.-90C>T
XR_241294.1:n.51C>T
NM_001037631.3:c.-90C>T	NP_001032720.1:n.-90C>T
NM_005214.5:c.-90C>T MANE Select	NP_005205.2:n.-90C>T