Canonical Allele Identifier: CA9226168

Gene: MAN2B1

Linked Data

• ClinVar Variation Id: 888937
• ClinVar RCV Id: RCV001122557
• dbSNP Id: rs749183690
• ExAC: 19:12760827 C / T
• gnomAD v2: 19-12760827-C-T
• gnomAD v3: 19-12650013-C-T
• gnomAD v4: 19-12650013-C-T
• MyVariant Identifiers: chr19:g.12760827C>T (hg19) ; chr19:g.12650013C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12650013C>T , CM000681.2:g.12650013C>T	GRCh38
NC_000019.9:g.12760827C>T , CM000681.1:g.12760827C>T	GRCh37
NC_000019.8:g.12621827C>T	NCBI36
NG_008318.1:g.21765G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.2167G>A MANE Select	ENSP00000395473.2:p.Asp723Asn
ENST00000221363.8:c.2164G>A	ENSP00000221363.4:p.Asp722Asn
ENST00000456935.6:c.2167G>A	ENSP00000395473.2:p.Asp723Asn
ENST00000466794.5:n.2757G>A
NM_000528.3:c.2167G>A	NP_000519.2:p.Asp723Asn
NM_001173498.1:c.2164G>A	NP_001166969.1:p.Asp722Asn
XM_005259913.1:c.2170G>A	XP_005259970.1:p.Asp724Asn
XM_011528017.1:c.1066G>A	XP_011526319.1:p.Asp356Asn
XM_005259913.2:c.2170G>A	XP_005259970.1:p.Asp724Asn
XM_024451518.1:c.1066G>A	XP_024307286.1:p.Asp356Asn
NM_000528.4:c.2167G>A MANE Select	NP_000519.2:p.Asp723Asn
NM_001173498.2:c.2164G>A	NP_001166969.1:p.Asp722Asn