Canonical Allele Identifier: CA631836053

Gene: MAN2B1

Linked Data

• ClinVar Variation Id: 1625329
• ClinVar RCV Id: RCV002130298
• dbSNP Id: rs754654189
• gnomAD v2: 19-12769344-A-G
• gnomAD v4: 19-12658530-A-G
• MyVariant Identifiers: chr19:g.12769344A>G (hg19) ; chr19:g.12658530A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12658530A>G , CM000681.2:g.12658530A>G	GRCh38
NC_000019.9:g.12769344A>G , CM000681.1:g.12769344A>G	GRCh37
NC_000019.8:g.12630344A>G	NCBI36
NG_008318.1:g.13248T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.1027-20T>C MANE Select	ENSP00000395473.2:n.1027-20T>C
ENST00000221363.8:c.1027-23T>C	ENSP00000221363.4:n.1027-23T>C
ENST00000456935.6:c.1027-20T>C	ENSP00000395473.2:n.1027-20T>C
ENST00000465830.1:n.88T>C
ENST00000466794.5:n.1009-186T>C
ENST00000495617.1:n.280+201T>C
NM_000528.3:c.1027-20T>C	NP_000519.2:n.1027-20T>C
NM_001173498.1:c.1027-23T>C	NP_001166969.1:n.1027-23T>C
XM_005259913.1:c.1027-17T>C	XP_005259970.1:n.1027-17T>C
XM_011528017.1:c.9-186T>C	XP_011526319.1:n.9-186T>C
XM_005259913.2:c.1027-17T>C	XP_005259970.1:n.1027-17T>C
XM_024451518.1:c.9-186T>C	XP_024307286.1:n.9-186T>C
NM_000528.4:c.1027-20T>C MANE Select	NP_000519.2:n.1027-20T>C
NM_001173498.2:c.1027-23T>C	NP_001166969.1:n.1027-23T>C