LDH info

Canonical Allele Identifier: CA9144989
Gene: FCER2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs28364072

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7690399A>G , CM000681.2:g.7690399A>G GRCh38
NC_000019.9:g.7755285A>G , CM000681.1:g.7755285A>G GRCh37
NC_000019.8:g.7661285A>G NCBI36
NG_029554.1:g.16748T>C

Transcript Alleles

HGVS Amino-acid change
NM_001207019.2:c.618+7T>C VV NP_001193948.2:p.=
NM_001220500.1:c.621+7T>C VV NP_001207429.1:p.=
NM_002002.4:c.621+7T>C VV NP_001993.2:p.=
XM_005272462.3:c.621+7T>C XP_005272519.1:p.=
XM_005272462.4:c.621+7T>C XP_005272519.1:p.=
NM_001220500.2:c.621+7T>C VV MANE Preferred NP_001207429.1:p.=
ENST00000346664.9:c.621+7T>C ENSP00000264072.6:p.=
ENST00000360067.8:c.618+7T>C ENSP00000353178.4:p.=
ENST00000597312.5:n.1146+7T>C
ENST00000597921.5:c.621+7T>C ENSP00000471974.1:p.=
ENST00000597934.1:n.983+7T>C
ENST00000598803.5:n.1116+7T>C