Canonical Allele Identifier: CA404248615

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12769261T>C (hg19) ; chr19:g.12658447T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12658447T>C , CM000681.2:g.12658447T>C	GRCh38
NC_000019.9:g.12769261T>C , CM000681.1:g.12769261T>C	GRCh37
NC_000019.8:g.12630261T>C	NCBI36
NG_008318.1:g.13331A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.1090A>G MANE Select	ENSP00000395473.2:p.Asn364Asp
ENST00000221363.8:c.1087A>G	ENSP00000221363.4:p.Asn363Asp
ENST00000456935.6:c.1090A>G	ENSP00000395473.2:p.Asn364Asp
ENST00000465830.1:n.171A>G
ENST00000466794.5:n.1009-103A>G
ENST00000495617.1:n.280+284A>G
NM_000528.3:c.1090A>G	NP_000519.2:p.Asn364Asp
NM_001173498.1:c.1087A>G	NP_001166969.1:p.Asn363Asp
XM_005259913.1:c.1093A>G	XP_005259970.1:p.Asn365Asp
XM_011528017.1:c.9-103A>G	XP_011526319.1:n.9-103A>G
XM_005259913.2:c.1093A>G	XP_005259970.1:p.Asn365Asp
XM_024451518.1:c.9-103A>G	XP_024307286.1:n.9-103A>G
NM_000528.4:c.1090A>G MANE Select	NP_000519.2:p.Asn364Asp
NM_001173498.2:c.1087A>G	NP_001166969.1:p.Asn363Asp