Canonical Allele Identifier: CA9226868

Gene: MAN2B1

Linked Data

• ClinVar Variation Id: 2896007
• ClinVar RCV Id: RCV003601028
• dbSNP Id: rs752981029
• ExAC: 19:12776500 C / T
• gnomAD v2: 19-12776500-C-T
• gnomAD v3: 19-12665686-C-T
• gnomAD v4: 19-12665686-C-T
• MyVariant Identifiers: chr19:g.12776500C>T (hg19) ; chr19:g.12665686C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12665686C>T , CM000681.2:g.12665686C>T	GRCh38
NC_000019.9:g.12776500C>T , CM000681.1:g.12776500C>T	GRCh37
NC_000019.8:g.12637500C>T	NCBI36
NG_008318.1:g.6092G>A
NG_015814.1:g.3883C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000456935.7:c.262+17G>A MANE Select	ENSP00000395473.2:n.262+17G>A
ENST00000221363.8:c.262+17G>A	ENSP00000221363.4:n.262+17G>A
ENST00000456935.6:c.262+17G>A	ENSP00000395473.2:n.262+17G>A
ENST00000466794.5:n.244+17G>A
ENST00000486847.2:c.160-161G>A	ENSP00000470174.1:n.160-161G>A
ENST00000596512.5:n.201-161G>A
ENST00000597961.1:c.253+17G>A	ENSP00000472710.1:n.253+17G>A
ENST00000598876.1:c.289+17G>A	ENSP00000470533.1:n.289+17G>A
ENST00000600281.1:n.303+17G>A
NM_000528.3:c.262+17G>A	NP_000519.2:n.262+17G>A
NM_001173498.1:c.262+17G>A	NP_001166969.1:n.262+17G>A
XM_005259913.1:c.262+17G>A	XP_005259970.1:n.262+17G>A
XM_005259913.2:c.262+17G>A	XP_005259970.1:n.262+17G>A
XM_024451518.1:c.-757+17G>A	XP_024307286.1:n.-757+17G>A
NM_000528.4:c.262+17G>A MANE Select	NP_000519.2:n.262+17G>A
NM_001173498.2:c.262+17G>A	NP_001166969.1:n.262+17G>A