Canonical Allele Identifier: CA404237853

Gene: MAN2B1

Linked Data

• gnomAD v4: 19-12647499-C-G
• MyVariant Identifiers: chr19:g.12758313C>G (hg19) ; chr19:g.12647499C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12647499C>G , CM000681.2:g.12647499C>G	GRCh38
NC_000019.9:g.12758313C>G , CM000681.1:g.12758313C>G	GRCh37
NC_000019.8:g.12619313C>G	NCBI36
NG_008318.1:g.24279G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.2764G>C MANE Select	ENSP00000395473.2:p.Ala922Pro
ENST00000221363.8:c.2761G>C	ENSP00000221363.4:p.Ala921Pro
ENST00000456935.6:c.2764G>C	ENSP00000395473.2:p.Ala922Pro
ENST00000466794.5:n.3354G>C
ENST00000469423.1:n.86G>C
ENST00000493218.5:n.175G>C
ENST00000597692.1:c.323G>C
NM_000528.3:c.2764G>C	NP_000519.2:p.Ala922Pro
NM_001173498.1:c.2761G>C	NP_001166969.1:p.Ala921Pro
XM_005259913.1:c.2767G>C	XP_005259970.1:p.Ala923Pro
XM_011528017.1:c.1663G>C	XP_011526319.1:p.Ala555Pro
XM_005259913.2:c.2767G>C	XP_005259970.1:p.Ala923Pro
XM_024451518.1:c.1663G>C	XP_024307286.1:p.Ala555Pro
NM_000528.4:c.2764G>C MANE Select	NP_000519.2:p.Ala922Pro
NM_001173498.2:c.2761G>C	NP_001166969.1:p.Ala921Pro