LDH info

Canonical Allele Identifier: CA3709725
Gene: TCF19 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2073724

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31161930C>T , CM000668.2:g.31161930C>T GRCh38
NC_000006.11:g.31129707C>T , CM000668.1:g.31129707C>T GRCh37
NC_000006.10:g.31237686C>T NCBI36
NG_054878.1:g.1309G>A

Transcript Alleles

HGVS Amino-acid change
NM_001077511.1:c.722C>T VV NP_001070979.1:p.Pro241Leu
NM_007109.2:c.722C>T VV NP_009040.2:p.Pro241Leu
XM_005249334.2:c.722C>T XP_005249391.1:p.Pro241Leu
XM_011514829.1:c.722C>T XP_011513131.1:p.Pro241Leu
NM_001318908.1:c.722C>T VV NP_001305837.1:p.Pro241Leu
NM_007109.3:c.722C>T VV MANE Preferred NP_009040.2:p.Pro241Leu
ENST00000376255.4:c.722C>T ENSP00000365431.4:p.Pro241Leu
ENST00000376257.7:c.722C>T ENSP00000365433.3:p.Pro241Leu
ENST00000496421.1:n.274C>T
ENST00000542218.1:n.482C>T ENSP00000439397.1:p.Pro161Leu