LDH info

Canonical Allele Identifier: CA2440753
Gene: STAB1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1010553

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52506757T>C , CM000665.2:g.52506757T>C GRCh38
NC_000003.11:g.52540773T>C , CM000665.1:g.52540773T>C GRCh37
NC_000003.10:g.52515813T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_015136.2:c.1896T>C VV NP_055951.2:p.Gly632=
XM_005264973.2:c.1896T>C XP_005265030.1:p.Gly632=
XM_005264974.2:c.1896T>C XP_005265031.1:p.Gly632=
XM_005264975.2:c.1896T>C XP_005265032.1:p.Gly632=
XM_006713065.1:c.1896T>C XP_006713128.1:p.Gly632=
XM_011533528.1:c.1896T>C XP_011531830.1:p.Gly632=
XR_940395.1:n.1972T>C
XM_005264973.3:c.1896T>C XP_005265030.1:p.Gly632=
XM_017005998.1:c.1896T>C XP_016861487.1:p.Gly632=
XM_017005999.1:c.1896T>C XP_016861488.1:p.Gly632=
XM_017006000.1:c.1896T>C XP_016861489.1:p.Gly632=
XM_017006001.1:c.1896T>C XP_016861490.1:p.Gly632=
XM_017006002.1:c.1896T>C XP_016861491.1:p.Gly632=
XM_017006003.1:c.1896T>C XP_016861492.1:p.Gly632=
XM_017006004.2:c.1896T>C XP_016861493.1:p.Gly632=
XR_001740064.1:n.1972T>C
NM_015136.3:c.1896T>C VV MANE Preferred NP_055951.2:p.Gly632=
ENST00000321725.10:c.1896T>C ENSP00000312946.6:p.Gly632=
ENST00000481607.1:n.1951T>C