Canonical Allele Identifier: CA2362416911
Gene: MROH8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.37137936A= , CM000682.2:g.37137936A= GRCh38
NC_000020.10:g.35766339A= , CM000682.1:g.35766339A= GRCh37
NC_000020.9:g.35199753A= NCBI36
NG_033795.1:g.46682T=
NG_033795.2:g.46642T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343811.10:c.1523T= ENSP00000513568.1:p.Leu508=
ENST00000400440.7:c.1523T= ENSP00000513569.1:p.Leu508=
ENST00000421643.2:c.1418T= ENSP00000513570.1:p.Leu473=
ENST00000422138.2:c.1265T= ENSP00000400468.2:p.Leu422=
ENST00000343811.9:n.1592T=
ENST00000343811.8:c.1603T=
ENST00000400440.6:c.1615T=
ENST00000400441.7:c.1523T= ENSP00000383291.4:p.Leu508=
ENST00000417458.5:c.405T=
ENST00000421643.1:c.1527T=