Canonical Allele Identifier: CA404237757

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12758289T>C (hg19) ; chr19:g.12647475T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12647475T>C , CM000681.2:g.12647475T>C	GRCh38
NC_000019.9:g.12758289T>C , CM000681.1:g.12758289T>C	GRCh37
NC_000019.8:g.12619289T>C	NCBI36
NG_008318.1:g.24303A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000456935.7:c.2788A>G MANE Select	ENSP00000395473.2:p.Asn930Asp
ENST00000221363.8:c.2785A>G	ENSP00000221363.4:p.Asn929Asp
ENST00000456935.6:c.2788A>G	ENSP00000395473.2:p.Asn930Asp
ENST00000466794.5:n.3378A>G
ENST00000469423.1:n.110A>G
ENST00000493218.5:n.199A>G
ENST00000597692.1:c.347A>G
NM_000528.3:c.2788A>G	NP_000519.2:p.Asn930Asp
NM_001173498.1:c.2785A>G	NP_001166969.1:p.Asn929Asp
XM_005259913.1:c.2791A>G	XP_005259970.1:p.Asn931Asp
XM_011528017.1:c.1687A>G	XP_011526319.1:p.Asn563Asp
XM_005259913.2:c.2791A>G	XP_005259970.1:p.Asn931Asp
XM_024451518.1:c.1687A>G	XP_024307286.1:p.Asn563Asp
NM_000528.4:c.2788A>G MANE Select	NP_000519.2:p.Asn930Asp
NM_001173498.2:c.2785A>G	NP_001166969.1:p.Asn929Asp