Canonical Allele Identifier: CA408834275

Gene: MROH8

Linked Data

• MyVariant Identifiers: chr20:g.35766347A>T (hg19) ; chr20:g.37137944A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.37137944A>T , CM000682.2:g.37137944A>T	GRCh38
NC_000020.10:g.35766347A>T , CM000682.1:g.35766347A>T	GRCh37
NC_000020.9:g.35199761A>T	NCBI36
NG_033795.1:g.46674T>A
NG_033795.2:g.46634T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000343811.10:c.1515T>A	ENSP00000513568.1:p.Cys505Ter
ENST00000400440.7:c.1515T>A	ENSP00000513569.1:p.Cys505Ter
ENST00000421643.2:c.1410T>A	ENSP00000513570.1:p.Cys470Ter
ENST00000422138.2:c.1257T>A	ENSP00000400468.2:p.Cys419Ter
ENST00000343811.9:n.1584T>A
ENST00000343811.8:c.1595T>A
ENST00000400440.6:c.1607T>A
ENST00000400441.7:c.1515T>A	ENSP00000383291.4:p.Cys505Ter
ENST00000417458.5:c.397T>A
ENST00000421643.1:c.1519T>A