Canonical Allele Identifier: CA763554950

Gene: CTLA4

Linked Data

• dbSNP Id: rs1180889903
• gnomAD v3: 2-203871528-A-G
• gnomAD v4: 2-203871528-A-G
• MyVariant Identifiers: chr2:g.204736251A>G (hg19) ; chr2:g.203871528A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203871528A>G , CM000664.2:g.203871528A>G	GRCh38
NC_000002.11:g.204736251A>G , CM000664.1:g.204736251A>G	GRCh37
NC_000002.10:g.204444496A>G	NCBI36
NG_011502.1:g.8743A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696049.1:c.507+101A>G	ENSP00000512353.1:n.507+101A>G
ENST00000696479.1:c.639+41A>G	ENSP00000512655.1:n.639+41A>G
ENST00000427473.3:n.491+595A>G
ENST00000648405.2:c.567+41A>G MANE Select	ENSP00000497102.1:n.567+41A>G
ENST00000650075.1:n.591+41A>G
ENST00000295854.10:c.457+595A>G	ENSP00000295854.6:n.457+595A>G
ENST00000302823.7:c.567+41A>G	ENSP00000303939.3:n.567+41A>G
ENST00000427473.2:c.346+595A>G	ENSP00000409707.2:n.346+595A>G
ENST00000472206.1:c.172+880A>G	ENSP00000417779.1:n.172+880A>G
ENST00000487393.1:n.110-1180A>G
NM_001037631.2:c.457+595A>G	NP_001032720.1:n.457+595A>G
NM_005214.4:c.567+41A>G	NP_005205.2:n.567+41A>G
XR_241294.1:n.707+41A>G
NM_001037631.3:c.457+595A>G	NP_001032720.1:n.457+595A>G
NM_005214.5:c.567+41A>G MANE Select	NP_005205.2:n.567+41A>G