Canonical Allele Identifier: CA763553024

Gene: CTLA4

Linked Data

• dbSNP Id: rs1254013363
• gnomAD v3: 2-203867829-G-A
• gnomAD v4: 2-203867829-G-A
• MyVariant Identifiers: chr2:g.204732552G>A (hg19) ; chr2:g.203867829G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203867829G>A , CM000664.2:g.203867829G>A	GRCh38
NC_000002.11:g.204732552G>A , CM000664.1:g.204732552G>A	GRCh37
NC_000002.10:g.204440797G>A	NCBI36
NG_011502.1:g.5044G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000696049.1:c.-114G>A	ENSP00000512353.1:n.-114G>A
ENST00000696479.1:c.48-89G>A	ENSP00000512655.1:n.48-89G>A
ENST00000648405.2:c.-114G>A MANE Select	ENSP00000497102.1:n.-114G>A
ENST00000302823.7:c.-114G>A	ENSP00000303939.3:n.-114G>A
NM_001037631.2:c.-114G>A	NP_001032720.1:n.-114G>A
NM_005214.4:c.-114G>A	NP_005205.2:n.-114G>A
XR_241294.1:n.27G>A
NM_001037631.3:c.-114G>A	NP_001032720.1:n.-114G>A
NM_005214.5:c.-114G>A MANE Select	NP_005205.2:n.-114G>A