LDH info

Canonical Allele Identifier: CA57289622
Gene: LRP1B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10210358

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.141038051A>G , CM000664.2:g.141038051A>G GRCh38
NC_000002.11:g.141795620A>G , CM000664.1:g.141795620A>G GRCh37
NC_000002.10:g.141512090A>G NCBI36
NG_051023.1:g.1099413T>C

Transcript Alleles

HGVS Amino-acid change
NM_018557.2:c.1789+10935T>C VV NP_061027.2:p.=
XM_011511352.1:c.1900+10935T>C XP_011509654.1:p.=
XM_017004341.1:c.1399+10935T>C XP_016859830.1:p.=
XR_001738778.1:n.3523+10935T>C
NM_018557.3:c.1789+10935T>C VV MANE Preferred NP_061027.2:p.=
ENST00000389484.7:c.1789+10935T>C ENSP00000374135.3:p.=
ENST00000434794.1:c.206-55775T>C ENSP00000413239.1:p.=
ENST00000618808.4:n.1447+10935T>C ENSP00000478868.1:p.=