LDH info

Canonical Allele Identifier: CA14128517
Gene: OCA2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs4778137

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.28082689C>G , CM000677.2:g.28082689C>G GRCh38
NC_000015.9:g.28327835C>G , CM000677.1:g.28327835C>G GRCh37
NC_000015.8:g.26001430C>G NCBI36
NG_009846.1:g.21624G>C

Transcript Alleles

HGVS Amino-acid change
NM_000275.2:c.-21-794G>C VV NP_000266.2:p.=
NM_001300984.1:c.-21-794G>C VV NP_001287913.1:p.=
XM_011521639.1:c.3+238G>C XP_011519941.1:p.=
XM_011521640.1:c.-21-794G>C XP_011519942.1:p.=
XM_011521641.1:c.3+238G>C XP_011519943.1:p.=
XM_011521642.1:c.3+238G>C XP_011519944.1:p.=
XM_011521643.1:c.3+238G>C XP_011519945.1:p.=
XM_011521644.1:c.3+238G>C XP_011519946.1:p.=
XM_011521645.1:c.3+238G>C XP_011519947.1:p.=
XM_011521646.1:c.3+238G>C XP_011519948.1:p.=
XM_011521647.1:c.3+238G>C XP_011519949.1:p.=
XR_931843.1:n.1364+238G>C
XM_011521640.2:c.-21-794G>C XP_011519942.1:p.=
XM_017022255.1:c.3+238G>C XP_016877744.1:p.=
XM_017022256.1:c.3+238G>C XP_016877745.1:p.=
XM_017022257.1:c.3+238G>C XP_016877746.1:p.=
XM_017022258.1:c.3+238G>C XP_016877747.1:p.=
XM_017022259.1:c.3+238G>C XP_016877748.1:p.=
XM_017022260.1:c.3+238G>C XP_016877749.1:p.=
XM_017022262.1:c.3+238G>C XP_016877751.1:p.=
XM_017022263.1:c.3+238G>C XP_016877752.1:p.=
XM_017022264.1:c.3+238G>C XP_016877753.1:p.=
XM_017022265.1:c.3+238G>C XP_016877754.1:p.=
XR_001751294.1:n.92+238G>C
NM_000275.3:c.-21-794G>C VV MANE Preferred NP_000266.2:p.=
NM_001300984.2:c.-21-794G>C VV NP_001287913.1:p.=
ENST00000353809.9:c.-21-794G>C ENSP00000261276.8:p.=
ENST00000354638.7:c.-21-794G>C ENSP00000346659.3:p.=
ENST00000431101.1:c.-21-794G>C ENSP00000415431.1:p.=
ENST00000445578.5:c.-21-794G>C ENSP00000414425.1:p.=