LDH info

Canonical Allele Identifier: CA212873
Gene: MCM6 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 7686
ClinVar RCV Id: RCV000008125
dbSNP Id: rs182549

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135859184C>T , CM000664.2:g.135859184C>T GRCh38
NC_000002.11:g.136616754C>T , CM000664.1:g.136616754C>T GRCh37
NC_000002.10:g.136333224C>T NCBI36
NG_008104.2:g.986G>A , LRG_338:g.986G>A
NG_008958.1:g.22258G>A

Transcript Alleles

HGVS Amino-acid change
NM_005915.5:c.1362+117G>A VV NP_005906.2:p.=
NM_005915.6:c.1362+117G>A VV MANE Preferred NP_005906.2:p.=
ENST00000264156.2:c.1362+117G>A ENSP00000264156.2:p.=
ENST00000492091.1:n.181+3423G>A