LDH info

Canonical Allele Identifier: CA1653482
Gene: LHCGR HGNC NCBI
STON1-GTF2A1L HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs4073366

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.48755483C>G , CM000664.2:g.48755483C>G GRCh38
NC_000002.11:g.48982622C>G , CM000664.1:g.48982622C>G GRCh37
NC_000002.10:g.48836126C>G NCBI36
NG_008193.1:g.5259G>C
NG_033050.1:g.230559C>G
NG_008193.2:g.5259G>C
NG_033050.2:g.230559C>G

Transcript Alleles

HGVS Amino-acid change
NM_000233.3:c.161+28G>C (LHCGR) VV NP_000224.2:p.=
NM_001198593.1:c.3442-20797C>G (STON1-GTF2A1L) VV NP_001185522.1:p.=
XM_011532828.1:c.161+28G>C (LHCGR) XP_011531130.1:p.=
XM_011532829.1:c.161+28G>C (LHCGR) XP_011531131.1:p.=
XM_011532830.1:c.161+28G>C (LHCGR) XP_011531132.1:p.=
NM_000233.4:c.161+28G>C (LHCGR) VV NP_000224.2:p.=
ENST00000294954.11:c.161+28G>C ENSP00000294954.6:p.=
ENST00000401907.5:c.161+28G>C ENSP00000385406.1:p.=
ENST00000402114.6:c.3442-20797C>G ENSP00000385701.1:p.=
ENST00000403273.5:c.161+28G>C ENSP00000385847.1:p.=
ENST00000405626.5:n.161+28G>C ENSP00000386033.1:p.=
ENST00000428232.2:n.59+28G>C ENSP00000403748.1:p.=
ENST00000602369.3:c.161+28G>C ENSP00000473498.1:p.=