LDH info

Canonical Allele Identifier: CA6243494
Gene: PGR HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1042839

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.101051471G>A , CM000673.2:g.101051471G>A GRCh38
NC_000011.9:g.100922202G>A , CM000673.1:g.100922202G>A GRCh37
NC_000011.8:g.100427412G>A NCBI36
NG_016475.1:g.83343C>T

Transcript Alleles

HGVS Amino-acid change
NM_000926.4:c.2310C>T VV MANE Preferred NP_000917.3:p.His770=
NM_001202474.3:c.1818C>T VV NP_001189403.1:p.His606=
NM_001271161.2:c.1512C>T VV NP_001258090.1:p.His504=
NM_001271162.1:c.528C>T VV NP_001258091.1:p.His176=
NR_073141.2:n.2303C>T
NR_073142.2:n.2186C>T
NR_073143.2:n.1997C>T
XM_006718858.2:c.2310C>T XP_006718921.1:p.His770=
XM_006718858.3:c.2310C>T XP_006718921.1:p.His770=
NM_001271162.2:c.528C>T VV NP_001258091.1:p.His176=
ENST00000263463.9:n.2004C>T ENSP00000263463.5:p.His668=
ENST00000325455.9:c.2310C>T ENSP00000325120.5:p.His770=
ENST00000526300.5:n.2004C>T ENSP00000436803.1:p.His668=
ENST00000528960.5:n.2193C>T ENSP00000432914.1:p.His731=
ENST00000533207.5:n.1677C>T
ENST00000534013.5:c.528C>T ENSP00000436561.1:p.His176=
ENST00000534780.5:n.2310C>T ENSP00000432352.1:p.His770=
ENST00000617858.4:c.2004C>T ENSP00000481227.1:p.His668=
ENST00000619228.2:c.2193C>T ENSP00000482698.1:p.His731=