Canonical Allele Identifier: CA404246329

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12767816A>C (hg19) ; chr19:g.12657002A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12657002A>C , CM000681.2:g.12657002A>C	GRCh38
NC_000019.9:g.12767816A>C , CM000681.1:g.12767816A>C	GRCh37
NC_000019.8:g.12628816A>C	NCBI36
NG_008318.1:g.14776T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.1474T>G MANE Select	ENSP00000395473.2:p.Phe492Val
ENST00000221363.8:c.1471T>G	ENSP00000221363.4:p.Phe491Val
ENST00000433513.5:n.80T>G
ENST00000456935.6:c.1474T>G	ENSP00000395473.2:p.Phe492Val
ENST00000466794.5:n.1373T>G
ENST00000495617.1:n.650T>G
ENST00000593686.1:c.84T>G
ENST00000595880.5:n.71T>G
NM_000528.3:c.1474T>G	NP_000519.2:p.Phe492Val
NM_001173498.1:c.1471T>G	NP_001166969.1:p.Phe491Val
XM_005259913.1:c.1477T>G	XP_005259970.1:p.Phe493Val
XM_011528017.1:c.373T>G	XP_011526319.1:p.Phe125Val
XM_005259913.2:c.1477T>G	XP_005259970.1:p.Phe493Val
XM_024451518.1:c.373T>G	XP_024307286.1:p.Phe125Val
NM_000528.4:c.1474T>G MANE Select	NP_000519.2:p.Phe492Val
NM_001173498.2:c.1471T>G	NP_001166969.1:p.Phe491Val