LDH info

Canonical Allele Identifier: CA15213031
Gene: CTLA4 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs231779

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203869764C>T , CM000664.2:g.203869764C>T GRCh38
NC_000002.11:g.204734487C>T , CM000664.1:g.204734487C>T GRCh37
NC_000002.10:g.204442732C>T NCBI36
NG_011502.1:g.6979C>T

Transcript Alleles

HGVS Amino-acid change
NM_001037631.2:c.110-822C>T VV NP_001032720.1:p.=
NM_005214.4:c.110-822C>T VV NP_005205.2:p.=
XR_241294.1:n.250-822C>T
NM_001037631.3:c.110-822C>T VV NP_001032720.1:p.=
NM_005214.5:c.110-822C>T VV MANE Preferred NP_005205.2:p.=
ENST00000295854.10:n.110-822C>T ENSP00000295854.6:p.=
ENST00000302823.7:c.110-822C>T ENSP00000303939.3:p.=
ENST00000472206.1:n.110-822C>T ENSP00000417779.1:p.=
ENST00000487393.1:n.109+1713C>T