Canonical Allele Identifier: CA408834269

Gene: MROH8

Linked Data

• MyVariant Identifiers: chr20:g.35766345G>T (hg19) ; chr20:g.37137942G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.37137942G>T , CM000682.2:g.37137942G>T	GRCh38
NC_000020.10:g.35766345G>T , CM000682.1:g.35766345G>T	GRCh37
NC_000020.9:g.35199759G>T	NCBI36
NG_033795.1:g.46676C>A
NG_033795.2:g.46636C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343811.10:c.1517C>A	ENSP00000513568.1:p.Ala506Asp
ENST00000400440.7:c.1517C>A	ENSP00000513569.1:p.Ala506Asp
ENST00000421643.2:c.1412C>A	ENSP00000513570.1:p.Ala471Asp
ENST00000422138.2:c.1259C>A	ENSP00000400468.2:p.Ala420Asp
ENST00000343811.9:n.1586C>A
ENST00000343811.8:c.1597C>A
ENST00000400440.6:c.1609C>A
ENST00000400441.7:c.1517C>A	ENSP00000383291.4:p.Ala506Asp
ENST00000417458.5:c.399C>A
ENST00000421643.1:c.1521C>A