LDH info

Canonical Allele Identifier: CA11786119
Gene: NFKB1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1005819

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.102583148C>T , CM000666.2:g.102583148C>T GRCh38
NC_000004.11:g.103504305C>T , CM000666.1:g.103504305C>T GRCh37
NC_000004.10:g.103723343C>T NCBI36
NG_050628.1:g.86820C>T

Transcript Alleles

HGVS Amino-acid change
NM_001165412.1:c.924+191C>T VV NP_001158884.1:p.=
NM_003998.3:c.927+191C>T VV NP_003989.2:p.=
XM_011532006.1:c.948+191C>T XP_011530308.1:p.=
XM_011532007.1:c.924+191C>T XP_011530309.1:p.=
XM_011532008.1:c.768+191C>T XP_011530310.1:p.=
XM_011532009.1:c.531+191C>T XP_011530311.1:p.=
NM_001319226.1:c.924+191C>T VV NP_001306155.1:p.=
XM_011532006.2:c.948+191C>T XP_011530308.1:p.=
XM_024454067.1:c.951+191C>T XP_024309835.1:p.=
XM_024454068.1:c.927+191C>T XP_024309836.1:p.=
XM_024454069.1:c.792+191C>T XP_024309837.1:p.=
NM_003998.4:c.927+191C>T VV MANE Preferred NP_003989.2:p.=
ENST00000226574.8:c.927+191C>T ENSP00000226574.4:p.=
ENST00000394820.8:c.924+191C>T ENSP00000378297.4:p.=
ENST00000505458.5:c.924+191C>T ENSP00000424790.1:p.=
ENST00000508584.1:c.306+191C>T ENSP00000424815.1:p.=
ENST00000600343.5:c.384+191C>T ENSP00000469340.1:p.=