Canonical Allele Identifier: CA539149119
Gene: CTLA4 HGNC NCBI

Linked Data

gnomAD v2: 2-204734413-C-A
MyVariant Identifiers: chr2:g.204734413C>A (hg19) chr2:g.203869690C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203869690C>A , CM000664.2:g.203869690C>A GRCh38
NC_000002.11:g.204734413C>A , CM000664.1:g.204734413C>A GRCh37
NC_000002.10:g.204442658C>A NCBI36
NG_011502.1:g.6905C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000696049.1:c.110-896C>A ENSP00000512353.1:n.110-896C>A
ENST00000696479.1:c.182-896C>A ENSP00000512655.1:n.182-896C>A
ENST00000648405.2:c.110-896C>A MANE Select ENSP00000497102.1:n.110-896C>A
ENST00000295854.10:c.110-896C>A ENSP00000295854.6:n.110-896C>A
ENST00000302823.7:c.110-896C>A ENSP00000303939.3:n.110-896C>A
ENST00000472206.1:c.110-896C>A ENSP00000417779.1:n.110-896C>A
ENST00000487393.1:n.109+1639C>A
NM_001037631.2:c.110-896C>A NP_001032720.1:n.110-896C>A
NM_005214.4:c.110-896C>A NP_005205.2:n.110-896C>A
XR_241294.1:n.250-896C>A
NM_001037631.3:c.110-896C>A NP_001032720.1:n.110-896C>A
NM_005214.5:c.110-896C>A MANE Select NP_005205.2:n.110-896C>A
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