Canonical Allele Identifier: CA9226201

Gene: MAN2B1

Linked Data

• ClinVar Variation Id: 1705127
• ClinVar RCV Id: RCV002281757
• dbSNP Id: rs764376758
• ExAC: 19:12760995 C / T
• gnomAD v2: 19-12760995-C-T
• gnomAD v4: 19-12650181-C-T
• MyVariant Identifiers: chr19:g.12760995C>T (hg19) ; chr19:g.12650181C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12650181C>T , CM000681.2:g.12650181C>T	GRCh38
NC_000019.9:g.12760995C>T , CM000681.1:g.12760995C>T	GRCh37
NC_000019.8:g.12621995C>T	NCBI36
NG_008318.1:g.21597G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.2088G>A MANE Select	ENSP00000395473.2:p.Trp696Ter
ENST00000221363.8:c.2085G>A	ENSP00000221363.4:p.Trp695Ter
ENST00000456935.6:c.2088G>A	ENSP00000395473.2:p.Trp696Ter
ENST00000466794.5:n.2678G>A
NM_000528.3:c.2088G>A	NP_000519.2:p.Trp696Ter
NM_001173498.1:c.2085G>A	NP_001166969.1:p.Trp695Ter
XM_005259913.1:c.2091G>A	XP_005259970.1:p.Trp697Ter
XM_011528017.1:c.987G>A	XP_011526319.1:p.Trp329Ter
XM_005259913.2:c.2091G>A	XP_005259970.1:p.Trp697Ter
XM_024451518.1:c.987G>A	XP_024307286.1:p.Trp329Ter
NM_000528.4:c.2088G>A MANE Select	NP_000519.2:p.Trp696Ter
NM_001173498.2:c.2085G>A	NP_001166969.1:p.Trp695Ter