Canonical Allele Identifier: CA9226882

Gene: MAN2B1

Linked Data

• ClinVar Variation Id: 2181377
• ClinVar RCV Id: RCV002595619
• dbSNP Id: rs774892701
• ExAC: 19:12776587 G / A
• gnomAD v2: 19-12776587-G-A
• gnomAD v4: 19-12665773-G-A
• MyVariant Identifiers: chr19:g.12776587G>A (hg19) ; chr19:g.12665773G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12665773G>A , CM000681.2:g.12665773G>A	GRCh38
NC_000019.9:g.12776587G>A , CM000681.1:g.12776587G>A	GRCh37
NC_000019.8:g.12637587G>A	NCBI36
NG_008318.1:g.6005C>T
NG_015814.1:g.3970G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.192C>T MANE Select	ENSP00000395473.2:p.Asn64=
ENST00000221363.8:c.192C>T	ENSP00000221363.4:p.Asn64=
ENST00000456935.6:c.192C>T	ENSP00000395473.2:p.Asn64=
ENST00000466794.5:n.174C>T
ENST00000486847.2:c.160-248C>T	ENSP00000470174.1:n.160-248C>T
ENST00000596512.5:n.201-248C>T
ENST00000597961.1:c.183C>T	ENSP00000472710.1:p.Asn61=
ENST00000598876.1:c.219C>T	ENSP00000470533.1:p.Asn73=
ENST00000600281.1:n.233C>T
NM_000528.3:c.192C>T	NP_000519.2:p.Asn64=
NM_001173498.1:c.192C>T	NP_001166969.1:p.Asn64=
XM_005259913.1:c.192C>T	XP_005259970.1:p.Asn64=
XM_005259913.2:c.192C>T	XP_005259970.1:p.Asn64=
XM_024451518.1:c.-827C>T	XP_024307286.1:n.-827C>T
NM_000528.4:c.192C>T MANE Select	NP_000519.2:p.Asn64=
NM_001173498.2:c.192C>T	NP_001166969.1:p.Asn64=