LDH info

Canonical Allele Identifier: CA15508347
Gene: AUTS2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10237317

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.70580955A>G , CM000669.2:g.70580955A>G GRCh38
NC_000007.13:g.70045941A>G , CM000669.1:g.70045941A>G GRCh37
NC_000007.12:g.69683877A>G NCBI36
NG_034133.1:g.987037A>G

Transcript Alleles

HGVS Amino-acid change
NM_001127231.2:c.691-117614A>G VV NP_001120703.1:p.=
NM_015570.3:c.691-117614A>G VV NP_056385.1:p.=
XM_011516010.1:c.691-117614A>G XP_011514312.1:p.=
XM_011516011.1:c.691-117614A>G XP_011514313.1:p.=
XM_011516012.1:c.691-117614A>G XP_011514314.1:p.=
XM_011516013.1:c.691-117614A>G XP_011514315.1:p.=
XM_011516014.1:c.691-117614A>G XP_011514316.1:p.=
XM_011516015.1:c.691-117614A>G XP_011514317.1:p.=
XM_011516016.1:c.400-117614A>G XP_011514318.1:p.=
XM_011516017.1:c.217-117614A>G XP_011514319.1:p.=
XM_011516018.1:c.190-117614A>G XP_011514320.1:p.=
XM_011516010.2:c.691-117614A>G XP_011514312.1:p.=
XM_011516011.2:c.691-117614A>G XP_011514313.1:p.=
XM_011516012.2:c.691-117614A>G XP_011514314.1:p.=
XM_011516013.2:c.691-117614A>G XP_011514315.1:p.=
XM_011516014.2:c.691-117614A>G XP_011514316.1:p.=
XM_011516017.2:c.217-117614A>G XP_011514319.1:p.=
XM_011516018.2:c.190-117614A>G XP_011514320.1:p.=
XM_017011951.2:c.691-117614A>G XP_016867440.1:p.=
ENST00000342771.8:c.691-117614A>G ENSP00000344087.4:p.=
ENST00000406775.6:c.691-117614A>G ENSP00000385263.2:p.=