LDH info

Canonical Allele Identifier: CA15224132
Gene: ARHGAP15 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10176394

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.143338805T>C , CM000664.2:g.143338805T>C GRCh38
NC_000002.11:g.144096374T>C , CM000664.1:g.144096374T>C GRCh37
NC_000002.10:g.143812844T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_018460.3:c.474+88205T>C VV NP_060930.3:p.=
XM_006712632.2:c.474+88205T>C XP_006712695.1:p.=
XM_011511479.1:c.474+88205T>C XP_011509781.1:p.=
XM_011511480.1:c.474+88205T>C XP_011509782.1:p.=
XM_011511481.1:c.474+88205T>C XP_011509783.1:p.=
XM_011511482.1:c.474+88205T>C XP_011509784.1:p.=
XM_011511483.1:c.240+88205T>C XP_011509785.1:p.=
XM_011511484.1:c.474+88205T>C XP_011509786.1:p.=
XM_011511479.2:c.474+88205T>C XP_011509781.1:p.=
XM_011511481.2:c.474+88205T>C XP_011509783.1:p.=
XM_011511482.2:c.474+88205T>C XP_011509784.1:p.=
XM_017004499.2:c.474+88205T>C XP_016859988.1:p.=
XM_017004500.2:c.345+88205T>C XP_016859989.1:p.=
XM_017004501.1:c.474+88205T>C XP_016859990.1:p.=
XR_001738850.1:n.560+88205T>C
NM_018460.4:c.474+88205T>C VV MANE Preferred NP_060930.3:p.=
ENST00000295095.10:c.474+88205T>C ENSP00000295095.6:p.=
ENST00000460776.5:n.422+88205T>C
ENST00000469117.5:n.205+88205T>C
ENST00000474474.5:n.238+88205T>C
ENST00000552641.5:n.542+88205T>C