Canonical Allele Identifier: CA404246319

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12767814A>T (hg19) ; chr19:g.12657000A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12657000A>T , CM000681.2:g.12657000A>T	GRCh38
NC_000019.9:g.12767814A>T , CM000681.1:g.12767814A>T	GRCh37
NC_000019.8:g.12628814A>T	NCBI36
NG_008318.1:g.14778T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.1476T>A MANE Select	ENSP00000395473.2:p.Phe492Leu
ENST00000221363.8:c.1473T>A	ENSP00000221363.4:p.Phe491Leu
ENST00000433513.5:n.82T>A
ENST00000456935.6:c.1476T>A	ENSP00000395473.2:p.Phe492Leu
ENST00000466794.5:n.1375T>A
ENST00000495617.1:n.652T>A
ENST00000593686.1:c.86T>A
ENST00000595880.5:n.73T>A
NM_000528.3:c.1476T>A	NP_000519.2:p.Phe492Leu
NM_001173498.1:c.1473T>A	NP_001166969.1:p.Phe491Leu
XM_005259913.1:c.1479T>A	XP_005259970.1:p.Phe493Leu
XM_011528017.1:c.375T>A	XP_011526319.1:p.Phe125Leu
XM_005259913.2:c.1479T>A	XP_005259970.1:p.Phe493Leu
XM_024451518.1:c.375T>A	XP_024307286.1:p.Phe125Leu
NM_000528.4:c.1476T>A MANE Select	NP_000519.2:p.Phe492Leu
NM_001173498.2:c.1473T>A	NP_001166969.1:p.Phe491Leu