Canonical Allele Identifier: CA763553597

Gene: CTLA4

Linked Data

• dbSNP Id: rs1378655520
• gnomAD v3: 2-203869886-A-T
• gnomAD v4: 2-203869886-A-T
• MyVariant Identifiers: chr2:g.204734609A>T (hg19) ; chr2:g.203869886A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203869886A>T , CM000664.2:g.203869886A>T	GRCh38
NC_000002.11:g.204734609A>T , CM000664.1:g.204734609A>T	GRCh37
NC_000002.10:g.204442854A>T	NCBI36
NG_011502.1:g.7101A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696049.1:c.110-700A>T	ENSP00000512353.1:n.110-700A>T
ENST00000696479.1:c.182-700A>T	ENSP00000512655.1:n.182-700A>T
ENST00000648405.2:c.110-700A>T MANE Select	ENSP00000497102.1:n.110-700A>T
ENST00000295854.10:c.110-700A>T	ENSP00000295854.6:n.110-700A>T
ENST00000302823.7:c.110-700A>T	ENSP00000303939.3:n.110-700A>T
ENST00000472206.1:c.110-700A>T	ENSP00000417779.1:n.110-700A>T
ENST00000487393.1:n.109+1835A>T
NM_001037631.2:c.110-700A>T	NP_001032720.1:n.110-700A>T
NM_005214.4:c.110-700A>T	NP_005205.2:n.110-700A>T
XR_241294.1:n.250-700A>T
NM_001037631.3:c.110-700A>T	NP_001032720.1:n.110-700A>T
NM_005214.5:c.110-700A>T MANE Select	NP_005205.2:n.110-700A>T