Canonical Allele Identifier: CA783349150

Gene: MAN2B1

Linked Data

• dbSNP Id: rs1325236365
• gnomAD v3: 19-12657941-C-T
• gnomAD v4: 19-12657941-C-T
• MyVariant Identifiers: chr19:g.12768755C>T (hg19) ; chr19:g.12657941C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12657941C>T , CM000681.2:g.12657941C>T	GRCh38
NC_000019.9:g.12768755C>T , CM000681.1:g.12768755C>T	GRCh37
NC_000019.8:g.12629755C>T	NCBI36
NG_008318.1:g.13837G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.1309+122G>A MANE Select	ENSP00000395473.2:n.1309+122G>A
ENST00000221363.8:c.1306+122G>A	ENSP00000221363.4:n.1306+122G>A
ENST00000456935.6:c.1309+122G>A	ENSP00000395473.2:n.1309+122G>A
ENST00000465830.1:n.473+122G>A
ENST00000466794.5:n.1208+122G>A
ENST00000495617.1:n.281-181G>A
NM_000528.3:c.1309+122G>A	NP_000519.2:n.1309+122G>A
NM_001173498.1:c.1306+122G>A	NP_001166969.1:n.1306+122G>A
XM_005259913.1:c.1312+122G>A	XP_005259970.1:n.1312+122G>A
XM_011528017.1:c.208+122G>A	XP_011526319.1:n.208+122G>A
XM_005259913.2:c.1312+122G>A	XP_005259970.1:n.1312+122G>A
XM_024451518.1:c.208+122G>A	XP_024307286.1:n.208+122G>A
NM_000528.4:c.1309+122G>A MANE Select	NP_000519.2:n.1309+122G>A
NM_001173498.2:c.1306+122G>A	NP_001166969.1:n.1306+122G>A