LDH info

Canonical Allele Identifier: CA276973303
Gene: CREBBP HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs130002

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3777930T>C , CM000678.2:g.3777930T>C GRCh38
NC_000016.9:g.3827931T>C , CM000678.1:g.3827931T>C GRCh37
NC_000016.8:g.3767932T>C NCBI36
NG_009873.1:g.107191A>G

Transcript Alleles

HGVS Amino-acid change
NM_001079846.1:c.1999+81A>G VV NP_001073315.1:p.=
NM_004380.2:c.2113+81A>G VV NP_004371.2:p.=
XM_005255124.3:c.2113+81A>G XP_005255181.1:p.=
XM_005255125.3:c.2113+81A>G XP_005255182.1:p.=
XM_006720848.2:c.2113+81A>G XP_006720911.1:p.=
XM_011522380.1:c.2059+81A>G XP_011520682.1:p.=
XM_011522381.1:c.1360+81A>G XP_011520683.1:p.=
XM_011522382.1:c.2113+81A>G XP_011520684.1:p.=
XM_005255124.4:c.2113+81A>G XP_005255181.1:p.=
XM_005255125.4:c.2113+81A>G XP_005255182.1:p.=
XM_006720848.3:c.2113+81A>G XP_006720911.1:p.=
XM_011522381.2:c.1360+81A>G XP_011520683.1:p.=
XM_011522382.3:c.2113+81A>G XP_011520684.1:p.=
XM_017022944.1:c.2113+81A>G XP_016878433.1:p.=
ENST00000262367.9:c.2113+81A>G ENSP00000262367.5:p.=
ENST00000382070.7:c.1999+81A>G ENSP00000371502.3:p.=
ENST00000570939.2:n.718+81A>G ENSP00000461002.2:p.=
ENST00000571826.5:n.162+81A>G
ENST00000572134.1:n.426+81A>G