Canonical Allele Identifier: CA404246214

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12767790G>C (hg19) ; chr19:g.12656976G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12656976G>C , CM000681.2:g.12656976G>C	GRCh38
NC_000019.9:g.12767790G>C , CM000681.1:g.12767790G>C	GRCh37
NC_000019.8:g.12628790G>C	NCBI36
NG_008318.1:g.14802C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.1500C>G MANE Select	ENSP00000395473.2:p.Ile500Met
ENST00000221363.8:c.1497C>G	ENSP00000221363.4:p.Ile499Met
ENST00000433513.5:n.106C>G
ENST00000456935.6:c.1500C>G	ENSP00000395473.2:p.Ile500Met
ENST00000466794.5:n.1399C>G
ENST00000495617.1:n.676C>G
ENST00000593686.1:c.110C>G
ENST00000595880.5:n.97C>G
NM_000528.3:c.1500C>G	NP_000519.2:p.Ile500Met
NM_001173498.1:c.1497C>G	NP_001166969.1:p.Ile499Met
XM_005259913.1:c.1503C>G	XP_005259970.1:p.Ile501Met
XM_011528017.1:c.399C>G	XP_011526319.1:p.Ile133Met
XM_005259913.2:c.1503C>G	XP_005259970.1:p.Ile501Met
XM_024451518.1:c.399C>G	XP_024307286.1:p.Ile133Met
NM_000528.4:c.1500C>G MANE Select	NP_000519.2:p.Ile500Met
NM_001173498.2:c.1497C>G	NP_001166969.1:p.Ile499Met