LDH info

Canonical Allele Identifier: CA9506011
Gene: APOE HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs12982192

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44908002T>C , CM000681.2:g.44908002T>C GRCh38
NC_000019.9:g.45411259T>C , CM000681.1:g.45411259T>C GRCh37
NC_000019.8:g.50103099T>C NCBI36
NG_007084.2:g.7221T>C

Transcript Alleles

HGVS Amino-acid change
NM_000041.3:c.236+50T>C VV NP_000032.1:p.=
NM_001302688.1:c.314+50T>C VV NP_001289617.1:p.=
NM_001302689.1:c.236+50T>C VV NP_001289618.1:p.=
NM_001302690.1:c.236+50T>C VV NP_001289619.1:p.=
NM_001302691.1:c.236+50T>C VV NP_001289620.1:p.=
NM_000041.4:c.236+50T>C VV MANE Preferred NP_000032.1:p.=
NM_001302688.2:c.314+50T>C VV NP_001289617.1:p.=
NM_001302689.2:c.236+50T>C VV NP_001289618.1:p.=
NM_001302691.2:c.236+50T>C VV NP_001289620.1:p.=
ENST00000252486.8:c.236+50T>C ENSP00000252486.3:p.=
ENST00000425718.1:c.236+50T>C ENSP00000410423.1:p.=
ENST00000434152.5:c.314+50T>C ENSP00000413653.2:p.=
ENST00000446996.5:c.236+50T>C ENSP00000413135.1:p.=