LDH info

Canonical Allele Identifier: CA10699289

Identifiers and link-outs to other resources

dbSNP Id: rs3024490

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.206771966A>C , CM000663.2:g.206771966A>C GRCh38
NC_000001.10:g.206945311A>C , CM000663.1:g.206945311A>C GRCh37
NC_000001.9:g.205011934A>C NCBI36
NG_012088.1:g.5529T>G

Transcript Alleles

HGVS Amino-acid change
NM_000572.2:c.165+305T>G (IL10) VV NP_000563.1:p.=
XM_011509506.1:c.165+305T>G (IL10) XP_011507808.1:p.=
NM_000572.3:c.165+305T>G (IL10) VV NP_000563.1:p.=
NM_153758.3:c.-35+888A>C (IL19) VV NP_715639.1:p.=
ENST00000423557.1:c.165+305T>G ENSP00000412237.1:p.=