LDH info

Canonical Allele Identifier: CA12501933
Gene: CHN2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1002630

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.29388454G>A , CM000669.2:g.29388454G>A GRCh38
NC_000007.13:g.29428070G>A , CM000669.1:g.29428070G>A GRCh37
NC_000007.12:g.29394595G>A NCBI36
NG_029365.2:g.246908G>A

Transcript Alleles

HGVS Amino-acid change
NM_001293069.1:c.370-5225G>A VV NP_001279998.1:p.=
NM_001293070.1:c.184-5225G>A VV NP_001279999.1:p.=
NM_001293071.1:c.40-5225G>A VV NP_001280000.1:p.=
NM_001293072.1:c.100-5225G>A VV NP_001280001.1:p.=
NM_004067.3:c.145-5225G>A VV NP_004058.1:p.=
XM_011515105.1:c.448-5225G>A XP_011513407.1:p.=
XM_011515106.1:c.409-5225G>A XP_011513408.1:p.=
XM_011515107.1:c.223-5225G>A XP_011513409.1:p.=
XM_011515108.1:c.145-5225G>A XP_011513410.1:p.=
XM_011515109.1:c.106-5225G>A XP_011513411.1:p.=
XM_011515110.1:c.67-5225G>A XP_011513412.1:p.=
XM_011515111.1:c.40-5225G>A XP_011513413.1:p.=
XM_011515112.1:c.448-5225G>A XP_011513414.1:p.=
XM_011515105.2:c.448-5225G>A XP_011513407.1:p.=
XM_011515106.2:c.409-5225G>A XP_011513408.1:p.=
XM_011515107.2:c.223-5225G>A XP_011513409.1:p.=
XM_017011721.1:c.466-5225G>A XP_016867210.1:p.=
XM_017011722.1:c.241-5225G>A XP_016867211.1:p.=
ENST00000222792.10:c.145-5225G>A ENSP00000222792.6:p.=
ENST00000409350.5:c.184-5225G>A ENSP00000386968.1:p.=
ENST00000409922.5:n.356-5225G>A
ENST00000409964.6:n.344-5225G>A
ENST00000412536.5:n.165-5225G>A
ENST00000435288.6:c.145-5225G>A ENSP00000400282.3:p.=
ENST00000439384.5:c.370-5225G>A ENSP00000409843.1:p.=
ENST00000474070.5:n.245-5225G>A
ENST00000478128.6:n.239-5225G>A
ENST00000482820.6:n.354-5225G>A
ENST00000495789.6:n.145-5225G>A ENSP00000438587.2:p.=
ENST00000539389.5:n.145-5225G>A ENSP00000440526.2:p.=
ENST00000539406.5:n.145-5225G>A ENSP00000444063.2:p.=