LDH info

Canonical Allele Identifier: CA10827741
Gene: FMN2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs17672135

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.240282296T>C , CM000663.2:g.240282296T>C GRCh38
NC_000001.10:g.240445596T>C , CM000663.1:g.240445596T>C GRCh37
NC_000001.9:g.238512219T>C NCBI36
NG_042054.1:g.195412T>C

Transcript Alleles

HGVS Amino-acid change
NM_001305424.1:c.4166-12526T>C VV NP_001292353.1:p.=
NM_020066.4:c.4154-12526T>C VV NP_064450.3:p.=
NM_001348094.1:c.2075-12526T>C VV NP_001335023.1:p.=
XM_017001837.1:c.4166-12526T>C XP_016857326.1:p.=
XM_017001840.2:c.2294-12526T>C XP_016857329.1:p.=
XM_017001841.2:c.2294-12526T>C XP_016857330.1:p.=
NM_020066.5:c.4154-12526T>C VV MANE Preferred NP_064450.3:p.=
NM_001305424.2:c.4166-12526T>C VV NP_001292353.1:p.=
NM_001348094.2:c.2075-12526T>C VV NP_001335023.1:p.=
ENST00000319653.13:c.4154-12526T>C ENSP00000318884.9:p.=
ENST00000441342.1:c.92-12526T>C ENSP00000388922.1:p.=
ENST00000463398.5:n.214-12526T>C