Canonical Allele Identifier: CA404248193

Gene: MAN2B1

Linked Data

• ClinVar Variation Id: 2760312
• ClinVar RCV Id: RCV003498593
• gnomAD v4: 19-12658298-G-A
• MyVariant Identifiers: chr19:g.12769112G>A (hg19) ; chr19:g.12658298G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12658298G>A , CM000681.2:g.12658298G>A	GRCh38
NC_000019.9:g.12769112G>A , CM000681.1:g.12769112G>A	GRCh37
NC_000019.8:g.12630112G>A	NCBI36
NG_008318.1:g.13480C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.1156C>T MANE Select	ENSP00000395473.2:p.Gln386Ter
ENST00000221363.8:c.1153C>T	ENSP00000221363.4:p.Gln385Ter
ENST00000456935.6:c.1156C>T	ENSP00000395473.2:p.Gln386Ter
ENST00000465830.1:n.320C>T
ENST00000466794.5:n.1055C>T
ENST00000495617.1:n.280+433C>T
NM_000528.3:c.1156C>T	NP_000519.2:p.Gln386Ter
NM_001173498.1:c.1153C>T	NP_001166969.1:p.Gln385Ter
XM_005259913.1:c.1159C>T	XP_005259970.1:p.Gln387Ter
XM_011528017.1:c.55C>T	XP_011526319.1:p.Gln19Ter
XM_005259913.2:c.1159C>T	XP_005259970.1:p.Gln387Ter
XM_024451518.1:c.55C>T	XP_024307286.1:p.Gln19Ter
NM_000528.4:c.1156C>T MANE Select	NP_000519.2:p.Gln386Ter
NM_001173498.2:c.1153C>T	NP_001166969.1:p.Gln385Ter