Canonical Allele Identifier: CA408834262

Gene: MROH8

Linked Data

• MyVariant Identifiers: chr20:g.35766341C>A (hg19) ; chr20:g.37137938C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.37137938C>A , CM000682.2:g.37137938C>A	GRCh38
NC_000020.10:g.35766341C>A , CM000682.1:g.35766341C>A	GRCh37
NC_000020.9:g.35199755C>A	NCBI36
NG_033795.1:g.46680G>T
NG_033795.2:g.46640G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343811.10:c.1521G>T	ENSP00000513568.1:p.Gln507His
ENST00000400440.7:c.1521G>T	ENSP00000513569.1:p.Gln507His
ENST00000421643.2:c.1416G>T	ENSP00000513570.1:p.Gln472His
ENST00000422138.2:c.1263G>T	ENSP00000400468.2:p.Gln421His
ENST00000343811.9:n.1590G>T
ENST00000343811.8:c.1601G>T
ENST00000400440.6:c.1613G>T
ENST00000400441.7:c.1521G>T	ENSP00000383291.4:p.Gln507His
ENST00000417458.5:c.403G>T
ENST00000421643.1:c.1525G>T