Canonical Allele Identifier: CA404248148

Gene: MAN2B1

Linked Data

• gnomAD v4: 19-12658292-A-T
• MyVariant Identifiers: chr19:g.12769106A>T (hg19) ; chr19:g.12658292A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12658292A>T , CM000681.2:g.12658292A>T	GRCh38
NC_000019.9:g.12769106A>T , CM000681.1:g.12769106A>T	GRCh37
NC_000019.8:g.12630106A>T	NCBI36
NG_008318.1:g.13486T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.1162T>A MANE Select	ENSP00000395473.2:p.Trp388Arg
ENST00000221363.8:c.1159T>A	ENSP00000221363.4:p.Trp387Arg
ENST00000456935.6:c.1162T>A	ENSP00000395473.2:p.Trp388Arg
ENST00000465830.1:n.326T>A
ENST00000466794.5:n.1061T>A
ENST00000495617.1:n.280+439T>A
NM_000528.3:c.1162T>A	NP_000519.2:p.Trp388Arg
NM_001173498.1:c.1159T>A	NP_001166969.1:p.Trp387Arg
XM_005259913.1:c.1165T>A	XP_005259970.1:p.Trp389Arg
XM_011528017.1:c.61T>A	XP_011526319.1:p.Trp21Arg
XM_005259913.2:c.1165T>A	XP_005259970.1:p.Trp389Arg
XM_024451518.1:c.61T>A	XP_024307286.1:p.Trp21Arg
NM_000528.4:c.1162T>A MANE Select	NP_000519.2:p.Trp388Arg
NM_001173498.2:c.1159T>A	NP_001166969.1:p.Trp387Arg