Canonical Allele Identifier: CA408834252

Gene: MROH8

Linked Data

• gnomAD v3: 20-37137934-A-T
• gnomAD v4: 20-37137934-A-T
• MyVariant Identifiers: chr20:g.35766337A>T (hg19) ; chr20:g.37137934A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.37137934A>T , CM000682.2:g.37137934A>T	GRCh38
NC_000020.10:g.35766337A>T , CM000682.1:g.35766337A>T	GRCh37
NC_000020.9:g.35199751A>T	NCBI36
NG_033795.1:g.46684T>A
NG_033795.2:g.46644T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343811.10:c.1525T>A	ENSP00000513568.1:p.Ser509Thr
ENST00000400440.7:c.1525T>A	ENSP00000513569.1:p.Ser509Thr
ENST00000421643.2:c.1420T>A	ENSP00000513570.1:p.Ser474Thr
ENST00000422138.2:c.1267T>A	ENSP00000400468.2:p.Ser423Thr
ENST00000343811.9:n.1594T>A
ENST00000343811.8:c.1605T>A
ENST00000400440.6:c.1617T>A
ENST00000400441.7:c.1525T>A	ENSP00000383291.4:p.Ser509Thr
ENST00000417458.5:c.407T>A
ENST00000421643.1:c.1529T>A