LDH info

Canonical Allele Identifier: CA15317949
Gene: ARHGAP24 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs7660702

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.85730311T>C , CM000666.2:g.85730311T>C GRCh38
NC_000004.11:g.86651464T>C , CM000666.1:g.86651464T>C GRCh37
NC_000004.10:g.86870488T>C NCBI36
NG_051627.1:g.260181T>C

Transcript Alleles

HGVS Amino-acid change
NM_001025616.2:c.268+8339T>C VV NP_001020787.2:p.=
XM_005263263.3:c.268+8339T>C XP_005263320.1:p.=
XM_024454238.1:c.-18+8339T>C XP_024310006.1:p.=
XM_024454239.1:c.-18+8339T>C XP_024310007.1:p.=
NM_001025616.3:c.268+8339T>C VV MANE Preferred NP_001020787.2:p.=
ENST00000395184.5:c.268+8339T>C ENSP00000378611.1:p.=
ENST00000503995.5:c.268+8339T>C ENSP00000423206.1:p.=
ENST00000512201.5:c.-18+8339T>C ENSP00000426105.1:p.=