Canonical Allele Identifier: CA404256486

Gene: MAN2B1

Linked Data

• dbSNP Id: rs1362644583
• gnomAD v2: 19-12776237-G-A
• gnomAD v4: 19-12665423-G-A
• MyVariant Identifiers: chr19:g.12776237G>A (hg19) ; chr19:g.12665423G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12665423G>A , CM000681.2:g.12665423G>A	GRCh38
NC_000019.9:g.12776237G>A , CM000681.1:g.12776237G>A	GRCh37
NC_000019.8:g.12637237G>A	NCBI36
NG_008318.1:g.6355C>T
NG_015814.1:g.3620G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.365C>T MANE Select	ENSP00000395473.2:p.Ala122Val
ENST00000221363.8:c.365C>T	ENSP00000221363.4:p.Ala122Val
ENST00000456935.6:c.365C>T	ENSP00000395473.2:p.Ala122Val
ENST00000466794.5:n.347C>T
ENST00000486847.2:c.262C>T	ENSP00000470174.1:p.Pro88Ser
ENST00000596512.5:n.303C>T
ENST00000597961.1:c.356C>T	ENSP00000472710.1:p.Ala119Val
ENST00000598876.1:c.392C>T	ENSP00000470533.1:p.Ala131Val
ENST00000600281.1:n.406C>T
NM_000528.3:c.365C>T	NP_000519.2:p.Ala122Val
NM_001173498.1:c.365C>T	NP_001166969.1:p.Ala122Val
XM_005259913.1:c.365C>T	XP_005259970.1:p.Ala122Val
XM_005259913.2:c.365C>T	XP_005259970.1:p.Ala122Val
XM_024451518.1:c.-654C>T	XP_024307286.1:n.-654C>T
NM_000528.4:c.365C>T MANE Select	NP_000519.2:p.Ala122Val
NM_001173498.2:c.365C>T	NP_001166969.1:p.Ala122Val