Canonical Allele Identifier: CA408834254

Gene: MROH8

Linked Data

• MyVariant Identifiers: chr20:g.35766338T>G (hg19) ; chr20:g.37137935T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.37137935T>G , CM000682.2:g.37137935T>G	GRCh38
NC_000020.10:g.35766338T>G , CM000682.1:g.35766338T>G	GRCh37
NC_000020.9:g.35199752T>G	NCBI36
NG_033795.1:g.46683A>C
NG_033795.2:g.46643A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343811.10:c.1524A>C	ENSP00000513568.1:p.Leu508Phe
ENST00000400440.7:c.1524A>C	ENSP00000513569.1:p.Leu508Phe
ENST00000421643.2:c.1419A>C	ENSP00000513570.1:p.Leu473Phe
ENST00000422138.2:c.1266A>C	ENSP00000400468.2:p.Leu422Phe
ENST00000343811.9:n.1593A>C
ENST00000343811.8:c.1604A>C
ENST00000400440.6:c.1616A>C
ENST00000400441.7:c.1524A>C	ENSP00000383291.4:p.Leu508Phe
ENST00000417458.5:c.406A>C
ENST00000421643.1:c.1528A>C