Canonical Allele Identifier: CA404244792

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12766563G>C (hg19) ; chr19:g.12655749G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12655749G>C , CM000681.2:g.12655749G>C	GRCh38
NC_000019.9:g.12766563G>C , CM000681.1:g.12766563G>C	GRCh37
NC_000019.8:g.12627563G>C	NCBI36
NG_008318.1:g.16029C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000456935.7:c.1775C>G MANE Select	ENSP00000395473.2:p.Ala592Gly
ENST00000221363.8:c.1772C>G	ENSP00000221363.4:p.Ala591Gly
ENST00000433513.5:n.381C>G
ENST00000456935.6:c.1775C>G	ENSP00000395473.2:p.Ala592Gly
ENST00000466794.5:n.2365C>G
ENST00000593686.1:c.368C>G
ENST00000595880.5:n.372C>G
ENST00000596591.1:c.139C>G
NM_000528.3:c.1775C>G	NP_000519.2:p.Ala592Gly
NM_001173498.1:c.1772C>G	NP_001166969.1:p.Ala591Gly
XM_005259913.1:c.1778C>G	XP_005259970.1:p.Ala593Gly
XM_011528017.1:c.674C>G	XP_011526319.1:p.Ala225Gly
XM_005259913.2:c.1778C>G	XP_005259970.1:p.Ala593Gly
XM_024451518.1:c.674C>G	XP_024307286.1:p.Ala225Gly
NM_000528.4:c.1775C>G MANE Select	NP_000519.2:p.Ala592Gly
NM_001173498.2:c.1772C>G	NP_001166969.1:p.Ala591Gly