Canonical Allele Identifier: CA404237351

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12758092G>A (hg19) ; chr19:g.12647278G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12647278G>A , CM000681.2:g.12647278G>A	GRCh38
NC_000019.9:g.12758092G>A , CM000681.1:g.12758092G>A	GRCh37
NC_000019.8:g.12619092G>A	NCBI36
NG_008318.1:g.24500C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.2878C>T MANE Select	ENSP00000395473.2:p.Gln960Ter
ENST00000221363.8:c.2875C>T	ENSP00000221363.4:p.Gln959Ter
ENST00000456935.6:c.2878C>T	ENSP00000395473.2:p.Gln960Ter
ENST00000466794.5:n.3468C>T
ENST00000469423.1:n.307C>T
ENST00000493218.5:n.289C>T
ENST00000597692.1:c.437C>T
NM_000528.3:c.2878C>T	NP_000519.2:p.Gln960Ter
NM_001173498.1:c.2875C>T	NP_001166969.1:p.Gln959Ter
XM_005259913.1:c.2881C>T	XP_005259970.1:p.Gln961Ter
XM_011528017.1:c.1777C>T	XP_011526319.1:p.Gln593Ter
XM_005259913.2:c.2881C>T	XP_005259970.1:p.Gln961Ter
XM_024451518.1:c.1777C>T	XP_024307286.1:p.Gln593Ter
NM_000528.4:c.2878C>T MANE Select	NP_000519.2:p.Gln960Ter
NM_001173498.2:c.2875C>T	NP_001166969.1:p.Gln959Ter