Canonical Allele Identifier: CA305479055

Gene: MAN2B1

Linked Data

• ClinVar Variation Id: 2777311
• ClinVar RCV Id: RCV003600493
• dbSNP Id: rs769498383
• gnomAD v2: 19-12776626-A-G
• gnomAD v3: 19-12665812-A-G
• gnomAD v4: 19-12665812-A-G
• MyVariant Identifiers: chr19:g.12776626A>G (hg19) ; chr19:g.12665812A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12665812A>G , CM000681.2:g.12665812A>G	GRCh38
NC_000019.9:g.12776626A>G , CM000681.1:g.12776626A>G	GRCh37
NC_000019.8:g.12637626A>G	NCBI36
NG_008318.1:g.5966T>C
NG_015814.1:g.4009A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.160-7T>C MANE Select	ENSP00000395473.2:n.160-7T>C
ENST00000221363.8:c.160-7T>C	ENSP00000221363.4:n.160-7T>C
ENST00000456935.6:c.160-7T>C	ENSP00000395473.2:n.160-7T>C
ENST00000466794.5:n.142-7T>C
ENST00000486847.2:c.160-287T>C	ENSP00000470174.1:n.160-287T>C
ENST00000596512.5:n.201-287T>C
ENST00000597961.1:c.151-7T>C	ENSP00000472710.1:n.151-7T>C
ENST00000598876.1:c.180T>C	ENSP00000470533.1:p.Pro60=
ENST00000600281.1:n.201-7T>C
NM_000528.3:c.160-7T>C	NP_000519.2:n.160-7T>C
NM_001173498.1:c.160-7T>C	NP_001166969.1:n.160-7T>C
XM_005259913.1:c.160-7T>C	XP_005259970.1:n.160-7T>C
XM_005259913.2:c.160-7T>C	XP_005259970.1:n.160-7T>C
XM_024451518.1:c.-859-7T>C	XP_024307286.1:n.-859-7T>C
NM_000528.4:c.160-7T>C MANE Select	NP_000519.2:n.160-7T>C
NM_001173498.2:c.160-7T>C	NP_001166969.1:n.160-7T>C