Canonical Allele Identifier: CA505770830

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12758404C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12647590C>G , CM000681.2:g.12647590C>G	GRCh38
NC_000019.9:g.12758404C>G , CM000681.1:g.12758404C>G	GRCh37
NC_000019.8:g.12619404C>G	NCBI36
NG_008318.1:g.24188G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.2673G>C MANE Select	ENSP00000395473.2:p.Gly891=
ENST00000221363.8:c.2670G>C	ENSP00000221363.4:p.Gly890=
ENST00000456935.6:c.2673G>C	ENSP00000395473.2:p.Gly891=
ENST00000466794.5:n.3263G>C
ENST00000493218.5:n.84G>C
ENST00000597692.1:c.232G>C
NM_000528.3:c.2673G>C	NP_000519.2:p.Gly891=
NM_001173498.1:c.2670G>C	NP_001166969.1:p.Gly890=
XM_005259913.1:c.2676G>C	XP_005259970.1:p.Gly892=
XM_011528017.1:c.1572G>C	XP_011526319.1:p.Gly524=
XM_005259913.2:c.2676G>C	XP_005259970.1:p.Gly892=
XM_024451518.1:c.1572G>C	XP_024307286.1:p.Gly524=
NM_000528.4:c.2673G>C MANE Select	NP_000519.2:p.Gly891=
NM_001173498.2:c.2670G>C	NP_001166969.1:p.Gly890=