LDH info

Canonical Allele Identifier: CA12945218
Gene: FAM135B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11166827

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.138492027C>T , CM000670.2:g.138492027C>T GRCh38
NC_000008.10:g.139504270C>T , CM000670.1:g.139504270C>T GRCh37
NC_000008.9:g.139573452C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_015912.3:c.-20+4644G>A VV NP_056996.2:p.=
XM_011517061.1:c.-165+4644G>A XP_011515363.1:p.=
XM_011517062.1:c.-20+4644G>A XP_011515364.1:p.=
NM_001362965.1:c.-20+5600G>A VV NP_001349894.1:p.=
XM_011517061.2:c.-165+4644G>A XP_011515363.1:p.=
NM_015912.4:c.-20+4644G>A VV MANE Preferred NP_056996.2:p.=
ENST00000276737.10:c.-20+4644G>A ENSP00000276737.6:p.=
ENST00000395297.5:c.-20+4644G>A ENSP00000378710.1:p.=