LDH info

Canonical Allele Identifier: CA119012
Gene: CYP1B1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 7736
ClinVar RCV Id: RCV000008175
dbSNP Id: rs72549389

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38075387A>G , CM000664.2:g.38075387A>G GRCh38
NC_000002.11:g.38302530A>G , CM000664.1:g.38302530A>G GRCh37
NC_000002.10:g.38156034A>G NCBI36
NG_008386.2:g.5715T>C

Transcript Alleles

HGVS Amino-acid change
NM_000104.3:c.2T>C VV
XM_011533236.1:n.1A>G
ENST00000490576.1:c.2T>C
ENST00000494864.1:c.-70-4077T>C ENSP00000479876.1:p.=
ENST00000610745.4:c.2T>C
ENST00000613082.1:n.375+393T>C
ENST00000614273.1:c.2T>C