LDH info

Canonical Allele Identifier: CA308885969
Gene: APOE HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs387906568

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44909020C>G , CM000681.2:g.44909020C>G GRCh38
NC_000019.9:g.45412277C>G , CM000681.1:g.45412277C>G GRCh37
NC_000019.8:g.50104117C>G NCBI36
NG_007084.2:g.8239C>G

Transcript Alleles

HGVS Amino-acid change
NM_000041.3:c.724C>G VV NP_000032.1:p.Arg242Gly
NM_001302688.1:c.802C>G VV NP_001289617.1:p.Arg268Gly
NM_001302689.1:c.724C>G VV NP_001289618.1:p.Arg242Gly
NM_001302690.1:c.724C>G VV NP_001289619.1:p.Arg242Gly
NM_001302691.1:c.724C>G VV NP_001289620.1:p.Arg242Gly
NM_000041.4:c.724C>G VV MANE Preferred NP_000032.1:p.Arg242Gly
NM_001302688.2:c.802C>G VV NP_001289617.1:p.Arg268Gly
NM_001302689.2:c.724C>G VV NP_001289618.1:p.Arg242Gly
NM_001302691.2:c.724C>G VV NP_001289620.1:p.Arg242Gly
ENST00000252486.8:c.724C>G ENSP00000252486.3:p.Arg242Gly
ENST00000434152.5:c.802C>G ENSP00000413653.2:p.Arg268Gly