Canonical Allele Identifier: CA16607558

Gene: MIB1

Linked Data

• ClinVar Variation Id: 379846
• ClinVar RCV Id: RCV000442389
• dbSNP Id: rs1057520754
• MyVariant Identifiers: chr18:g.19378060G>A (hg19) ; chr18:g.21798099G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.21798099G>A , CM000680.2:g.21798099G>A	GRCh38
NC_000018.9:g.19378060G>A , CM000680.1:g.19378060G>A	GRCh37
NC_000018.8:g.17632058G>A	NCBI36
NG_033272.2:g.98143G>A , LRG_759:g.98143G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261537.7:c.1108G>A MANE Select	ENSP00000261537.6:p.Gly370Ser
ENST00000261537.6:c.1108G>A	ENSP00000261537.6:p.Gly370Ser
ENST00000577749.5:n.16G>A
ENST00000578646.5:n.1085G>A
NM_020774.3:c.1108G>A , LRG_759t1:c.1108G>A	NP_065825.1:p.Gly370Ser
XR_935234.1:n.1899G>A
XR_935235.1:n.1899G>A
XM_017025873.1:c.592G>A	XP_016881362.1:p.Gly198Ser
XM_017025874.1:c.1108G>A	XP_016881363.1:p.Gly370Ser
XM_017025875.1:c.1108G>A	XP_016881364.1:p.Gly370Ser
NM_020774.4:c.1108G>A MANE Select	NP_065825.1:p.Gly370Ser