LDH info

Canonical Allele Identifier: CA1408698
Gene: FAM177B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs6683071

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.222750009A>G , CM000663.2:g.222750009A>G GRCh38
NC_000001.10:g.222923351A>G , CM000663.1:g.222923351A>G GRCh37
NC_000001.9:g.220989974A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_207468.2:c.428A>G VV NP_997351.2:p.Gln143Arg
XM_006711318.2:c.241+2928A>G XP_006711381.1:p.=
NM_001324080.1:c.428A>G VV NP_001311009.1:p.Gln143Arg
NR_136691.1:n.1198A>G
XM_017001279.1:c.428A>G XP_016856768.1:p.Gln143Arg
XM_017001280.1:c.428A>G XP_016856769.1:p.Gln143Arg
XM_017001281.1:c.428A>G XP_016856770.1:p.Gln143Arg
XM_017001282.1:c.428A>G XP_016856771.1:p.Gln143Arg
XM_017001285.1:c.274+2928A>G XP_016856774.1:p.=
ENST00000360827.6:c.428A>G ENSP00000354070.2:p.Gln143Arg
ENST00000391880.6:c.*569A>G ENSP00000375752.2:p.=
ENST00000445590.3:c.428A>G ENSP00000414451.2:p.Gln143Arg