LDH info

Canonical Allele Identifier: CA13260794
Gene: CACNB2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs7076247

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.18470700T>C , CM000672.2:g.18470700T>C GRCh38
NC_000010.10:g.18759629T>C , CM000672.1:g.18759629T>C GRCh37
NC_000010.9:g.18799635T>C NCBI36
NG_016195.1:g.335024T>C

Transcript Alleles

HGVS Amino-acid change
NM_000724.3:c.169-27655T>C VV NP_000715.2:p.=
NM_001167945.1:c.250-27655T>C VV NP_001161417.1:p.=
NM_201570.2:c.190-27655T>C VV NP_963864.1:p.=
NM_201571.3:c.250-27655T>C VV NP_963865.2:p.=
NM_201572.3:c.250-27655T>C VV NP_963866.2:p.=
NM_201590.2:c.172-27655T>C VV NP_963884.2:p.=
NM_201593.2:c.334-27655T>C VV NP_963887.2:p.=
NM_201596.2:c.334-27655T>C VV NP_963890.2:p.=
NM_201597.2:c.334-27655T>C VV NP_963891.1:p.=
XM_005252588.2:c.190-27655T>C XP_005252645.1:p.=
XM_006717502.2:c.154-27655T>C XP_006717565.1:p.=
XM_011519659.1:c.172-27655T>C XP_011517961.1:p.=
XM_011519660.1:c.169-27655T>C XP_011517962.1:p.=
NM_001330060.1:c.169-27655T>C VV NP_001316989.1:p.=
XM_005252588.4:c.190-27655T>C XP_005252645.1:p.=
XM_006717502.3:c.154-27655T>C XP_006717565.1:p.=
XM_011519659.2:c.172-27655T>C XP_011517961.1:p.=
XM_017016625.1:c.-455-27655T>C XP_016872114.1:p.=
XR_001747198.1:n.511-27655T>C
NM_000724.4:c.169-27655T>C VV NP_000715.2:p.=
NM_001167945.2:c.250-27655T>C VV NP_001161417.1:p.=
NM_001330060.2:c.169-27655T>C VV NP_001316989.1:p.=
NM_201570.3:c.190-27655T>C VV NP_963864.1:p.=
NM_201571.4:c.250-27655T>C VV NP_963865.2:p.=
NM_201572.4:c.250-27655T>C VV NP_963866.2:p.=
NM_201590.3:c.172-27655T>C VV NP_963884.2:p.=
NM_201593.3:c.334-27655T>C VV NP_963887.2:p.=
NM_201596.3:c.334-27655T>C VV NP_963890.2:p.=
NM_201597.3:c.334-27655T>C VV NP_963891.1:p.=
ENST00000282343.12:c.250-27655T>C ENSP00000282343.8:p.=
ENST00000324631.11:c.334-27655T>C ENSP00000320025.7:p.=
ENST00000352115.10:n.334-27655T>C ENSP00000344474.6:p.=
ENST00000377315.4:c.190-27655T>C ENSP00000366532.4:p.=
ENST00000377319.7:c.169-27655T>C ENSP00000366536.3:p.=
ENST00000377328.5:n.334-27655T>C ENSP00000366545.1:p.=
ENST00000377329.8:c.172-27655T>C ENSP00000366546.4:p.=
ENST00000377331.6:n.250-27655T>C ENSP00000366548.2:p.=
ENST00000396576.6:c.169-27655T>C ENSP00000379821.2:p.=
ENST00000498816.1:n.382-27655T>C
ENST00000612134.4:n.172-27655T>C ENSP00000480563.1:p.=
ENST00000612743.1:c.35-68564T>C ENSP00000478676.1:p.=
ENST00000615785.4:c.169-27655T>C ENSP00000480260.1:p.=
ENST00000617363.4:c.169-27655T>C ENSP00000479756.1:p.=