Canonical Allele Identifier: CA305479035

Gene: MAN2B1

Linked Data

• ClinVar Variation Id: 1098035
• ClinVar RCV Id: RCV001419848
• dbSNP Id: rs1043541354
• gnomAD v2: 19-12776599-C-T
• gnomAD v3: 19-12665785-C-T
• gnomAD v4: 19-12665785-C-T
• COSMIC: COSM1390615
• MyVariant Identifiers: chr19:g.12776599C>T (hg19) ; chr19:g.12665785C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12665785C>T , CM000681.2:g.12665785C>T	GRCh38
NC_000019.9:g.12776599C>T , CM000681.1:g.12776599C>T	GRCh37
NC_000019.8:g.12637599C>T	NCBI36
NG_008318.1:g.5993G>A
NG_015814.1:g.3982C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.180G>A MANE Select	ENSP00000395473.2:p.Pro60=
ENST00000221363.8:c.180G>A	ENSP00000221363.4:p.Pro60=
ENST00000456935.6:c.180G>A	ENSP00000395473.2:p.Pro60=
ENST00000466794.5:n.162G>A
ENST00000486847.2:c.160-260G>A	ENSP00000470174.1:n.160-260G>A
ENST00000596512.5:n.201-260G>A
ENST00000597961.1:c.171G>A	ENSP00000472710.1:p.Pro57=
ENST00000598876.1:c.207G>A	ENSP00000470533.1:p.Pro69=
ENST00000600281.1:n.221G>A
NM_000528.3:c.180G>A	NP_000519.2:p.Pro60=
NM_001173498.1:c.180G>A	NP_001166969.1:p.Pro60=
XM_005259913.1:c.180G>A	XP_005259970.1:p.Pro60=
XM_005259913.2:c.180G>A	XP_005259970.1:p.Pro60=
XM_024451518.1:c.-839G>A	XP_024307286.1:n.-839G>A
NM_000528.4:c.180G>A MANE Select	NP_000519.2:p.Pro60=
NM_001173498.2:c.180G>A	NP_001166969.1:p.Pro60=