Canonical Allele Identifier: CA305478963

Gene: MAN2B1

Linked Data

• dbSNP Id: rs777622062
• gnomAD v4: 19-12665583-A-G
• MyVariant Identifiers: chr19:g.12776397A>G (hg19) ; chr19:g.12665583A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12665583A>G , CM000681.2:g.12665583A>G	GRCh38
NC_000019.9:g.12776397A>G , CM000681.1:g.12776397A>G	GRCh37
NC_000019.8:g.12637397A>G	NCBI36
NG_008318.1:g.6195T>C
NG_015814.1:g.3780A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.263-58T>C MANE Select	ENSP00000395473.2:n.263-58T>C
ENST00000221363.8:c.263-58T>C	ENSP00000221363.4:n.263-58T>C
ENST00000456935.6:c.263-58T>C	ENSP00000395473.2:n.263-58T>C
ENST00000466794.5:n.245-58T>C
ENST00000486847.2:c.160-58T>C	ENSP00000470174.1:n.160-58T>C
ENST00000596512.5:n.201-58T>C
ENST00000597961.1:c.254-58T>C	ENSP00000472710.1:n.254-58T>C
ENST00000598876.1:c.290-58T>C	ENSP00000470533.1:n.290-58T>C
ENST00000600281.1:n.304-58T>C
NM_000528.3:c.263-58T>C	NP_000519.2:n.263-58T>C
NM_001173498.1:c.263-58T>C	NP_001166969.1:n.263-58T>C
XM_005259913.1:c.263-58T>C	XP_005259970.1:n.263-58T>C
XM_005259913.2:c.263-58T>C	XP_005259970.1:n.263-58T>C
XM_024451518.1:c.-756-58T>C	XP_024307286.1:n.-756-58T>C
NM_000528.4:c.263-58T>C MANE Select	NP_000519.2:n.263-58T>C
NM_001173498.2:c.263-58T>C	NP_001166969.1:n.263-58T>C