Canonical Allele Identifier: CA505770707

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12758308T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12647494T>A , CM000681.2:g.12647494T>A	GRCh38
NC_000019.9:g.12758308T>A , CM000681.1:g.12758308T>A	GRCh37
NC_000019.8:g.12619308T>A	NCBI36
NG_008318.1:g.24284A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.2769A>T MANE Select	ENSP00000395473.2:p.Val923=
ENST00000221363.8:c.2766A>T	ENSP00000221363.4:p.Val922=
ENST00000456935.6:c.2769A>T	ENSP00000395473.2:p.Val923=
ENST00000466794.5:n.3359A>T
ENST00000469423.1:n.91A>T
ENST00000493218.5:n.180A>T
ENST00000597692.1:c.328A>T
NM_000528.3:c.2769A>T	NP_000519.2:p.Val923=
NM_001173498.1:c.2766A>T	NP_001166969.1:p.Val922=
XM_005259913.1:c.2772A>T	XP_005259970.1:p.Val924=
XM_011528017.1:c.1668A>T	XP_011526319.1:p.Val556=
XM_005259913.2:c.2772A>T	XP_005259970.1:p.Val924=
XM_024451518.1:c.1668A>T	XP_024307286.1:p.Val556=
NM_000528.4:c.2769A>T MANE Select	NP_000519.2:p.Val923=
NM_001173498.2:c.2766A>T	NP_001166969.1:p.Val922=