Canonical Allele Identifier: CA2582722473

Gene: MAN2B1

Linked Data

• gnomAD v4: 19-12665124-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12665124T>G , CM000681.2:g.12665124T>G	GRCh38
NC_000019.9:g.12775938T>G , CM000681.1:g.12775938T>G	GRCh37
NC_000019.8:g.12636938T>G	NCBI36
NG_008318.1:g.6654A>C
NG_015814.1:g.3321T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.437-139A>C MANE Select	ENSP00000395473.2:n.437-139A>C
ENST00000221363.8:c.437-139A>C	ENSP00000221363.4:n.437-139A>C
ENST00000456935.6:c.437-139A>C	ENSP00000395473.2:n.437-139A>C
ENST00000466794.5:n.419-139A>C
ENST00000486847.2:c.333+228A>C	ENSP00000470174.1:n.333+228A>C
ENST00000596512.5:n.375-139A>C
ENST00000597961.1:c.428-139A>C	ENSP00000472710.1:n.428-139A>C
ENST00000598876.1:c.464-139A>C	ENSP00000470533.1:n.464-139A>C
NM_000528.3:c.437-139A>C	NP_000519.2:n.437-139A>C
NM_001173498.1:c.437-139A>C	NP_001166969.1:n.437-139A>C
XM_005259913.1:c.437-139A>C	XP_005259970.1:n.437-139A>C
XM_005259913.2:c.437-139A>C	XP_005259970.1:n.437-139A>C
XM_024451518.1:c.-582-139A>C	XP_024307286.1:n.-582-139A>C
NM_000528.4:c.437-139A>C MANE Select	NP_000519.2:n.437-139A>C
NM_001173498.2:c.437-139A>C	NP_001166969.1:n.437-139A>C