LDH info

Canonical Allele Identifier: CA14332968
Gene: CREBBP HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs129963

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3746146T>C , CM000678.2:g.3746146T>C GRCh38
NC_000016.9:g.3796147T>C , CM000678.1:g.3796147T>C GRCh37
NC_000016.8:g.3736148T>C NCBI36
NG_009873.1:g.138975A>G
NG_009873.2:g.139568A>G

Transcript Alleles

HGVS Amino-acid change
NM_001079846.1:c.3723-792A>G VV NP_001073315.1:p.=
NM_004380.2:c.3837-792A>G VV NP_004371.2:p.=
XM_005255124.3:c.3792-792A>G XP_005255181.1:p.=
XM_005255125.3:c.3420-792A>G XP_005255182.1:p.=
XM_006720848.2:c.3837-792A>G XP_006720911.1:p.=
XM_011522380.1:c.3783-792A>G XP_011520682.1:p.=
XM_011522381.1:c.3084-792A>G XP_011520683.1:p.=
XM_011522382.1:c.3837-551A>G XP_011520684.1:p.=
XM_005255124.4:c.3792-792A>G XP_005255181.1:p.=
XM_005255125.4:c.3420-792A>G XP_005255182.1:p.=
XM_006720848.3:c.3837-792A>G XP_006720911.1:p.=
XM_011522381.2:c.3084-792A>G XP_011520683.1:p.=
XM_011522382.3:c.3837-551A>G XP_011520684.1:p.=
XM_017022944.1:c.3831-792A>G XP_016878433.1:p.=
NM_004380.3:c.3837-792A>G VV MANE Preferred NP_004371.2:p.=
ENST00000262367.9:c.3837-792A>G ENSP00000262367.5:p.=
ENST00000382070.7:c.3723-792A>G ENSP00000371502.3:p.=
ENST00000570939.2:n.2472-792A>G ENSP00000461002.2:p.=
ENST00000573517.6:n.143-792A>G