LDH info

Canonical Allele Identifier: CA235819
Gene: ABCC2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 191014
dbSNP Id: rs786205465

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99818791G>T , CM000672.2:g.99818791G>T GRCh38
NC_000010.10:g.101578548G>T , CM000672.1:g.101578548G>T GRCh37
NC_000010.9:g.101568538G>T NCBI36
NG_011798.1:g.41086G>T
NG_011798.2:g.41194G>T

Transcript Alleles

HGVS Amino-acid change
NM_000392.4:c.2273G>T VV NP_000383.1:p.Gly758Val
XM_006717630.2:c.1577G>T XP_006717693.1:p.Gly526Val
XM_006717631.2:c.2273G>T XP_006717694.1:p.Gly758Val
XM_011539291.1:c.2273G>T XP_011537593.1:p.Gly758Val
XR_945604.1:n.2462G>T
XR_945605.1:n.2464G>T
NM_000392.5:c.2273G>T VV NP_000383.2:p.Gly758Val
XM_006717630.3:c.1577G>T XP_006717693.1:p.Gly526Val
XM_006717631.4:c.2273G>T XP_006717694.1:p.Gly758Val
XM_011539291.3:c.2273G>T XP_011537593.1:p.Gly758Val
XM_017015675.2:c.2273G>T XP_016871164.1:p.Gly758Val
XR_945604.3:n.2516G>T
XR_945605.3:n.2516G>T
ENST00000370449.8:c.2273G>T ENSP00000359478.4:p.Gly758Val