LDH info

Canonical Allele Identifier: CA876022
Gene: C8B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1013579

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.56956811C>T , CM000663.2:g.56956811C>T GRCh38
NC_000001.10:g.57422484C>T , CM000663.1:g.57422484C>T GRCh37
NC_000001.9:g.57195072C>T NCBI36
NG_007285.1:g.14205G>A , LRG_31:g.14205G>A

Transcript Alleles

HGVS Amino-acid change
XM_017002235.1:c.349G>A XP_016857724.1:p.Gly117Arg
XR_001737397.1:n.449G>A
NM_000066.4:c.349G>A VV MANE Preferred NP_000057.3:p.Gly117Arg
ENST00000371237.8:c.349G>A ENSP00000360281.4:p.Gly117Arg
ENST00000535057.5:c.163G>A ENSP00000440113.1:p.Gly55Arg
ENST00000543257.5:c.193G>A ENSP00000442548.1:p.Gly65Arg