LDH info

Canonical Allele Identifier: CA13485007
Gene: FADS2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1535

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61830500A>G , CM000673.2:g.61830500A>G GRCh38
NC_000011.9:g.61597972A>G , CM000673.1:g.61597972A>G GRCh37
NC_000011.8:g.61354548A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001281501.1:c.142-7278A>G VV NP_001268430.1:p.=
NM_001281502.1:c.115-7278A>G VV NP_001268431.1:p.=
NM_004265.3:c.207+1903A>G VV NP_004256.1:p.=
XM_011545395.1:c.207+1903A>G XP_011543697.1:p.=
NM_004265.4:c.207+1903A>G VV MANE Preferred NP_004256.1:p.=
ENST00000257261.10:c.142-7278A>G ENSP00000257261.6:p.=
ENST00000278840.8:c.207+1903A>G ENSP00000278840.4:p.=
ENST00000517312.5:c.-160+1903A>G ENSP00000430225.1:p.=
ENST00000518606.5:c.-160+3069A>G ENSP00000430054.1:p.=
ENST00000521849.5:c.207+1903A>G ENSP00000431091.1:p.=
ENST00000522056.5:c.115-7278A>G ENSP00000429500.1:p.=