LDH info

Canonical Allele Identifier: CA337454856
Gene: ZFY HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2267802

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2960384A>G , CM000686.2:g.2960384A>G GRCh38
NC_000024.9:g.2828425A>G , CM000686.1:g.2828425A>G GRCh37
NC_000024.8:g.2888425A>G NCBI36
NG_008113.1:g.29880A>G

Transcript Alleles

HGVS Amino-acid change
NM_001145275.1:c.-17-690A>G VV NP_001138747.1:p.=
NM_001145276.1:c.61+6387A>G VV NP_001138748.1:p.=
NM_003411.3:c.62-690A>G VV NP_003402.2:p.=
XM_005262570.2:c.62-690A>G XP_005262627.1:p.=
XM_006724873.2:c.62-690A>G XP_006724936.1:p.=
XM_011531473.1:c.-17-690A>G XP_011529775.1:p.=
XM_011531474.1:c.-17-690A>G XP_011529776.1:p.=
XM_011531475.1:c.62-690A>G XP_011529777.1:p.=
XM_011531473.2:c.-17-690A>G XP_011529775.1:p.=
XM_011531474.2:c.-17-690A>G XP_011529776.1:p.=
XM_011531475.3:c.62-690A>G XP_011529777.1:p.=
XM_017030075.1:c.62-690A>G XP_016885564.1:p.=
XM_017030076.1:c.62-690A>G XP_016885565.1:p.=
XM_017030077.1:c.-17-690A>G XP_016885566.1:p.=
NM_003411.4:c.62-690A>G VV MANE Preferred NP_003402.2:p.=
ENST00000155093.7:c.62-690A>G ENSP00000155093.3:p.=
ENST00000383052.5:c.62-690A>G ENSP00000372525.1:p.=
ENST00000443793.1:c.62-690A>G ENSP00000388814.1:p.=
ENST00000449237.4:c.-17-690A>G ENSP00000393908.1:p.=
ENST00000469869.1:n.271-14711A>G
ENST00000625061.3:c.61+6387A>G ENSP00000485605.1:p.=