Canonical Allele Identifier: CA505770835

Gene: MAN2B1

Linked Data

• gnomAD v4: 19-12647596-G-A
• MyVariant Identifiers: chr19:g.12758410G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12647596G>A , CM000681.2:g.12647596G>A	GRCh38
NC_000019.9:g.12758410G>A , CM000681.1:g.12758410G>A	GRCh37
NC_000019.8:g.12619410G>A	NCBI36
NG_008318.1:g.24182C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.2667C>T MANE Select	ENSP00000395473.2:p.Phe889=
ENST00000221363.8:c.2664C>T	ENSP00000221363.4:p.Phe888=
ENST00000456935.6:c.2667C>T	ENSP00000395473.2:p.Phe889=
ENST00000466794.5:n.3257C>T
ENST00000493218.5:n.78C>T
ENST00000597692.1:c.226C>T
NM_000528.3:c.2667C>T	NP_000519.2:p.Phe889=
NM_001173498.1:c.2664C>T	NP_001166969.1:p.Phe888=
XM_005259913.1:c.2670C>T	XP_005259970.1:p.Phe890=
XM_011528017.1:c.1566C>T	XP_011526319.1:p.Phe522=
XM_005259913.2:c.2670C>T	XP_005259970.1:p.Phe890=
XM_024451518.1:c.1566C>T	XP_024307286.1:p.Phe522=
NM_000528.4:c.2667C>T MANE Select	NP_000519.2:p.Phe889=
NM_001173498.2:c.2664C>T	NP_001166969.1:p.Phe888=