Canonical Allele Identifier: CA763554596

Gene: CTLA4

Linked Data

• dbSNP Id: rs1488301664
• gnomAD v3: 2-203871242-G-T
• gnomAD v4: 2-203871242-G-T
• MyVariant Identifiers: chr2:g.204735965G>T (hg19) ; chr2:g.203871242G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203871242G>T , CM000664.2:g.203871242G>T	GRCh38
NC_000002.11:g.204735965G>T , CM000664.1:g.204735965G>T	GRCh37
NC_000002.10:g.204444210G>T	NCBI36
NG_011502.1:g.8457G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696049.1:c.458-136G>T	ENSP00000512353.1:n.458-136G>T
ENST00000696479.1:c.530-136G>T	ENSP00000512655.1:n.530-136G>T
ENST00000427473.3:n.491+309G>T
ENST00000648405.2:c.458-136G>T MANE Select	ENSP00000497102.1:n.458-136G>T
ENST00000650075.1:n.482-136G>T
ENST00000295854.10:c.457+309G>T	ENSP00000295854.6:n.457+309G>T
ENST00000302823.7:c.458-136G>T	ENSP00000303939.3:n.458-136G>T
ENST00000427473.2:c.346+309G>T	ENSP00000409707.2:n.346+309G>T
ENST00000472206.1:c.172+594G>T	ENSP00000417779.1:n.172+594G>T
ENST00000487393.1:n.110-1466G>T
NM_001037631.2:c.457+309G>T	NP_001032720.1:n.457+309G>T
NM_005214.4:c.458-136G>T	NP_005205.2:n.458-136G>T
XR_241294.1:n.598-136G>T
NM_001037631.3:c.457+309G>T	NP_001032720.1:n.457+309G>T
NM_005214.5:c.458-136G>T MANE Select	NP_005205.2:n.458-136G>T