Canonical Allele Identifier: CA63784390

Gene: CTLA4

Linked Data

• dbSNP Id: rs906821132
• gnomAD v2: 2-204730861-G-C
• gnomAD v3: 2-203866138-G-C
• gnomAD v4: 2-203866138-G-C
• MyVariant Identifiers: chr2:g.204730861G>C (hg19) ; chr2:g.203866138G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203866138G>C , CM000664.2:g.203866138G>C	GRCh38
NC_000002.11:g.204730861G>C , CM000664.1:g.204730861G>C	GRCh37
NC_000002.10:g.204439106G>C	NCBI36
NG_011502.1:g.3353G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000696479.1:c.48-1780G>C	ENSP00000512655.1:n.48-1780G>C