LDH info

Canonical Allele Identifier: CA254232658
Gene: ABCC4 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs16950650

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.95123178C>T , CM000675.2:g.95123178C>T GRCh38
NC_000013.10:g.95775432C>T , CM000675.1:g.95775432C>T GRCh37
NC_000013.9:g.94573433C>T NCBI36
NG_050651.1:g.183269G>A

Transcript Alleles

HGVS Amino-acid change
NM_001105515.2:c.2456-7177G>A VV NP_001098985.1:p.=
NM_001301829.1:c.2315-7177G>A VV NP_001288758.1:p.=
NM_001301830.1:c.2231-7177G>A VV NP_001288759.1:p.=
NM_005845.4:c.2456-7177G>A VV NP_005836.2:p.=
XM_005254025.2:c.2327-7177G>A XP_005254082.1:p.=
XM_006719914.1:c.2366-7177G>A XP_006719977.1:p.=
XM_011521047.1:c.1907-7177G>A XP_011519349.1:p.=
XM_017020319.1:c.2327-7177G>A XP_016875808.1:p.=
XM_017020321.1:c.941-7177G>A XP_016875810.1:p.=
XM_017020322.1:c.2327-7177G>A XP_016875811.1:p.=
NM_001105515.3:c.2456-7177G>A VV NP_001098985.1:p.=
NM_001301829.2:c.2315-7177G>A VV NP_001288758.1:p.=
NM_001301830.2:c.2231-7177G>A VV NP_001288759.1:p.=
NM_005845.5:c.2456-7177G>A VV MANE Preferred NP_005836.2:p.=
ENST00000376887.8:c.2456-7177G>A ENSP00000366084.4:p.=
ENST00000536256.3:c.2231-7177G>A ENSP00000442024.1:p.=
ENST00000629385.1:c.2456-7177G>A ENSP00000487081.1:p.=