Canonical Allele Identifier: CA404241101

Gene: MAN2B1

Linked Data

• dbSNP Id: rs1195120196
• MyVariant Identifiers: chr19:g.12759987C>T (hg19) ; chr19:g.12649173C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12649173C>T , CM000681.2:g.12649173C>T	GRCh38
NC_000019.9:g.12759987C>T , CM000681.1:g.12759987C>T	GRCh37
NC_000019.8:g.12620987C>T	NCBI36
NG_008318.1:g.22605G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.2399G>A MANE Select	ENSP00000395473.2:p.Gly800Glu
ENST00000221363.8:c.2396G>A	ENSP00000221363.4:p.Gly799Glu
ENST00000456935.6:c.2399G>A	ENSP00000395473.2:p.Gly800Glu
ENST00000466794.5:n.2989G>A
NM_000528.3:c.2399G>A	NP_000519.2:p.Gly800Glu
NM_001173498.1:c.2396G>A	NP_001166969.1:p.Gly799Glu
XM_005259913.1:c.2402G>A	XP_005259970.1:p.Gly801Glu
XM_011528017.1:c.1298G>A	XP_011526319.1:p.Gly433Glu
XM_005259913.2:c.2402G>A	XP_005259970.1:p.Gly801Glu
XM_024451518.1:c.1298G>A	XP_024307286.1:p.Gly433Glu
NM_000528.4:c.2399G>A MANE Select	NP_000519.2:p.Gly800Glu
NM_001173498.2:c.2396G>A	NP_001166969.1:p.Gly799Glu