Canonical Allele Identifier: CA404237887

Gene: MAN2B1

Linked Data

• dbSNP Id: rs1386530532
• gnomAD v3: 19-12647506-G-T
• gnomAD v4: 19-12647506-G-T
• MyVariant Identifiers: chr19:g.12758320G>T (hg19) ; chr19:g.12647506G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12647506G>T , CM000681.2:g.12647506G>T	GRCh38
NC_000019.9:g.12758320G>T , CM000681.1:g.12758320G>T	GRCh37
NC_000019.8:g.12619320G>T	NCBI36
NG_008318.1:g.24272C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.2757C>A MANE Select	ENSP00000395473.2:p.His919Gln
ENST00000221363.8:c.2754C>A	ENSP00000221363.4:p.His918Gln
ENST00000456935.6:c.2757C>A	ENSP00000395473.2:p.His919Gln
ENST00000466794.5:n.3347C>A
ENST00000469423.1:n.79C>A
ENST00000493218.5:n.168C>A
ENST00000597692.1:c.316C>A
NM_000528.3:c.2757C>A	NP_000519.2:p.His919Gln
NM_001173498.1:c.2754C>A	NP_001166969.1:p.His918Gln
XM_005259913.1:c.2760C>A	XP_005259970.1:p.His920Gln
XM_011528017.1:c.1656C>A	XP_011526319.1:p.His552Gln
XM_005259913.2:c.2760C>A	XP_005259970.1:p.His920Gln
XM_024451518.1:c.1656C>A	XP_024307286.1:p.His552Gln
NM_000528.4:c.2757C>A MANE Select	NP_000519.2:p.His919Gln
NM_001173498.2:c.2754C>A	NP_001166969.1:p.His918Gln