Canonical Allele Identifier: CA404250731

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12772175T>C (hg19) ; chr19:g.12661361T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12661361T>C , CM000681.2:g.12661361T>C	GRCh38
NC_000019.9:g.12772175T>C , CM000681.1:g.12772175T>C	GRCh37
NC_000019.8:g.12633175T>C	NCBI36
NG_008318.1:g.10417A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.925A>G MANE Select	ENSP00000395473.2:p.Thr309Ala
ENST00000221363.8:c.925A>G	ENSP00000221363.4:p.Thr309Ala
ENST00000456935.6:c.925A>G	ENSP00000395473.2:p.Thr309Ala
ENST00000462144.1:n.118A>G
ENST00000466794.5:n.907A>G
NM_000528.3:c.925A>G	NP_000519.2:p.Thr309Ala
NM_001173498.1:c.925A>G	NP_001166969.1:p.Thr309Ala
XM_005259913.1:c.925A>G	XP_005259970.1:p.Thr309Ala
XM_011528017.1:c.-94A>G	XP_011526319.1:n.-94A>G
XM_005259913.2:c.925A>G	XP_005259970.1:p.Thr309Ala
XM_024451518.1:c.-94A>G	XP_024307286.1:n.-94A>G
NM_000528.4:c.925A>G MANE Select	NP_000519.2:p.Thr309Ala
NM_001173498.2:c.925A>G	NP_001166969.1:p.Thr309Ala