LDH info

Canonical Allele Identifier: CA307703655
Gene: SCN1B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs104894718

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35033654C>T , CM000681.2:g.35033654C>T GRCh38
NC_000019.9:g.35524558C>T , CM000681.1:g.35524558C>T GRCh37
NC_000019.8:g.40216398C>T NCBI36
NG_013359.1:g.7967C>T

Transcript Alleles

HGVS Amino-acid change
NM_001037.4:c.363C>T VV NP_001028.1:p.Cys121=
NM_199037.3:c.363C>T VV NP_950238.1:p.Cys121=
XM_005259144.1:c.264C>T XP_005259201.1:p.Cys88=
NM_001321605.1:c.264C>T VV NP_001308534.1:p.Cys88=
NM_199037.4:c.363C>T VV NP_950238.1:p.Cys121=
NM_001037.5:c.363C>T VV MANE Preferred NP_001028.1:p.Cys121=
NM_001321605.2:c.264C>T VV NP_001308534.1:p.Cys88=
NM_199037.5:c.363C>T VV NP_950238.1:p.Cys121=
ENST00000262631.9:c.363C>T ENSP00000262631.3:p.Cys121=
ENST00000415950.3:n.363C>T ENSP00000396915.2:p.Cys121=
ENST00000595652.5:c.208-58C>T ENSP00000468848.1:p.=
ENST00000596348.1:n.372C>T