Canonical Allele Identifier: CA404243573

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12761012G>C (hg19) ; chr19:g.12650198G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12650198G>C , CM000681.2:g.12650198G>C	GRCh38
NC_000019.9:g.12761012G>C , CM000681.1:g.12761012G>C	GRCh37
NC_000019.8:g.12622012G>C	NCBI36
NG_008318.1:g.21580C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.2071C>G MANE Select	ENSP00000395473.2:p.Gln691Glu
ENST00000221363.8:c.2068C>G	ENSP00000221363.4:p.Gln690Glu
ENST00000456935.6:c.2071C>G	ENSP00000395473.2:p.Gln691Glu
ENST00000466794.5:n.2661C>G
NM_000528.3:c.2071C>G	NP_000519.2:p.Gln691Glu
NM_001173498.1:c.2068C>G	NP_001166969.1:p.Gln690Glu
XM_005259913.1:c.2074C>G	XP_005259970.1:p.Gln692Glu
XM_011528017.1:c.970C>G	XP_011526319.1:p.Gln324Glu
XM_005259913.2:c.2074C>G	XP_005259970.1:p.Gln692Glu
XM_024451518.1:c.970C>G	XP_024307286.1:p.Gln324Glu
NM_000528.4:c.2071C>G MANE Select	NP_000519.2:p.Gln691Glu
NM_001173498.2:c.2068C>G	NP_001166969.1:p.Gln690Glu