LDH info

Canonical Allele Identifier: CA10782435
Gene: APOA2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs5085

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161222721C>G , CM000663.2:g.161222721C>G GRCh38
NC_000001.10:g.161192511C>G , CM000663.1:g.161192511C>G GRCh37
NC_000001.9:g.159459135C>G NCBI36
NG_012043.1:g.5908G>C

Transcript Alleles

HGVS Amino-acid change
NM_001643.1:c.185+197G>C VV NP_001634.1:p.=
NM_001643.2:c.185+197G>C VV MANE Preferred NP_001634.1:p.=
ENST00000367990.7:c.185+197G>C ENSP00000356969.3:p.=
ENST00000463273.5:c.185+197G>C ENSP00000476740.1:p.=
ENST00000463812.1:c.41+197G>C ENSP00000476890.1:p.=
ENST00000464492.5:c.284+197G>C ENSP00000476911.1:p.=
ENST00000468465.5:c.41+197G>C ENSP00000476662.1:p.=
ENST00000469730.2:c.185+197G>C ENSP00000476605.1:p.=
ENST00000470459.6:c.185+197G>C ENSP00000477031.1:p.=
ENST00000481413.1:n.696+197G>C
ENST00000481511.5:c.*182+197G>C ENSP00000477054.1:p.=
ENST00000491350.1:c.53-199G>C ENSP00000477353.1:p.=