LDH info

Canonical Allele Identifier: CA212875
Gene: MCM6 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 7688
ClinVar RCV Id: RCV000008127
dbSNP Id: rs41380347

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135851081A>C , CM000664.2:g.135851081A>C GRCh38
NC_000002.11:g.136608651A>C , CM000664.1:g.136608651A>C GRCh37
NC_000002.10:g.136325121A>C NCBI36
NG_008104.2:g.9089T>G , LRG_338:g.9089T>G
NG_008958.1:g.30361T>G

Transcript Alleles

HGVS Amino-acid change
NM_005915.5:c.1917+321T>G VV NP_005906.2:p.=
NM_005915.6:c.1917+321T>G VV MANE Preferred NP_005906.2:p.=
ENST00000264156.2:c.1917+321T>G ENSP00000264156.2:p.=
ENST00000483902.1:n.544+321T>G
ENST00000492091.1:n.343+321T>G