Canonical Allele Identifier: CA505626785

Gene: MAN2B1

Linked Data

• gnomAD v4: 19-12665788-C-T
• MyVariant Identifiers: chr19:g.12776602C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12665788C>T , CM000681.2:g.12665788C>T	GRCh38
NC_000019.9:g.12776602C>T , CM000681.1:g.12776602C>T	GRCh37
NC_000019.8:g.12637602C>T	NCBI36
NG_008318.1:g.5990G>A
NG_015814.1:g.3985C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.177G>A MANE Select	ENSP00000395473.2:p.Gln59=
ENST00000221363.8:c.177G>A	ENSP00000221363.4:p.Gln59=
ENST00000456935.6:c.177G>A	ENSP00000395473.2:p.Gln59=
ENST00000466794.5:n.159G>A
ENST00000486847.2:c.160-263G>A	ENSP00000470174.1:n.160-263G>A
ENST00000596512.5:n.201-263G>A
ENST00000597961.1:c.168G>A	ENSP00000472710.1:p.Gln56=
ENST00000598876.1:c.204G>A	ENSP00000470533.1:p.Gln68=
ENST00000600281.1:n.218G>A
NM_000528.3:c.177G>A	NP_000519.2:p.Gln59=
NM_001173498.1:c.177G>A	NP_001166969.1:p.Gln59=
XM_005259913.1:c.177G>A	XP_005259970.1:p.Gln59=
XM_005259913.2:c.177G>A	XP_005259970.1:p.Gln59=
XM_024451518.1:c.-842G>A	XP_024307286.1:n.-842G>A
NM_000528.4:c.177G>A MANE Select	NP_000519.2:p.Gln59=
NM_001173498.2:c.177G>A	NP_001166969.1:p.Gln59=