Canonical Allele Identifier: CA404237768

Gene: MAN2B1

Linked Data

• dbSNP Id: rs142248782
• gnomAD v3: 19-12647478-G-C
• gnomAD v4: 19-12647478-G-C
• MyVariant Identifiers: chr19:g.12758292G>C (hg19) ; chr19:g.12647478G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12647478G>C , CM000681.2:g.12647478G>C	GRCh38
NC_000019.9:g.12758292G>C , CM000681.1:g.12758292G>C	GRCh37
NC_000019.8:g.12619292G>C	NCBI36
NG_008318.1:g.24300C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000456935.7:c.2785C>G MANE Select	ENSP00000395473.2:p.Arg929Gly
ENST00000221363.8:c.2782C>G	ENSP00000221363.4:p.Arg928Gly
ENST00000456935.6:c.2785C>G	ENSP00000395473.2:p.Arg929Gly
ENST00000466794.5:n.3375C>G
ENST00000469423.1:n.107C>G
ENST00000493218.5:n.196C>G
ENST00000597692.1:c.344C>G
NM_000528.3:c.2785C>G	NP_000519.2:p.Arg929Gly
NM_001173498.1:c.2782C>G	NP_001166969.1:p.Arg928Gly
XM_005259913.1:c.2788C>G	XP_005259970.1:p.Arg930Gly
XM_011528017.1:c.1684C>G	XP_011526319.1:p.Arg562Gly
XM_005259913.2:c.2788C>G	XP_005259970.1:p.Arg930Gly
XM_024451518.1:c.1684C>G	XP_024307286.1:p.Arg562Gly
NM_000528.4:c.2785C>G MANE Select	NP_000519.2:p.Arg929Gly
NM_001173498.2:c.2782C>G	NP_001166969.1:p.Arg928Gly