Canonical Allele Identifier: CA408834266

Gene: MROH8

Linked Data

• gnomAD v4: 20-37137940-G-C
• MyVariant Identifiers: chr20:g.35766343G>C (hg19) ; chr20:g.37137940G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.37137940G>C , CM000682.2:g.37137940G>C	GRCh38
NC_000020.10:g.35766343G>C , CM000682.1:g.35766343G>C	GRCh37
NC_000020.9:g.35199757G>C	NCBI36
NG_033795.1:g.46678C>G
NG_033795.2:g.46638C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000343811.10:c.1519C>G	ENSP00000513568.1:p.Gln507Glu
ENST00000400440.7:c.1519C>G	ENSP00000513569.1:p.Gln507Glu
ENST00000421643.2:c.1414C>G	ENSP00000513570.1:p.Gln472Glu
ENST00000422138.2:c.1261C>G	ENSP00000400468.2:p.Gln421Glu
ENST00000343811.9:n.1588C>G
ENST00000343811.8:c.1599C>G
ENST00000400440.6:c.1611C>G
ENST00000400441.7:c.1519C>G	ENSP00000383291.4:p.Gln507Glu
ENST00000417458.5:c.401C>G
ENST00000421643.1:c.1523C>G