Canonical Allele Identifier: CA993664450

Gene: MAN2B1

Linked Data

• dbSNP Id: rs2145223332
• gnomAD v3: 19-12647875-T-G
• gnomAD v4: 19-12647875-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12647875T>G , CM000681.2:g.12647875T>G	GRCh38
NC_000019.9:g.12758689T>G , CM000681.1:g.12758689T>G	GRCh37
NC_000019.8:g.12619689T>G	NCBI36
NG_008318.1:g.23903A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.2665-277A>C MANE Select	ENSP00000395473.2:n.2665-277A>C
ENST00000221363.8:c.2662-277A>C	ENSP00000221363.4:n.2662-277A>C
ENST00000456935.6:c.2665-277A>C	ENSP00000395473.2:n.2665-277A>C
ENST00000466794.5:n.3255-277A>C
ENST00000597692.1:c.224-277A>C
NM_000528.3:c.2665-277A>C	NP_000519.2:n.2665-277A>C
NM_001173498.1:c.2662-277A>C	NP_001166969.1:n.2662-277A>C
XM_005259913.1:c.2668-277A>C	XP_005259970.1:n.2668-277A>C
XM_011528017.1:c.1564-277A>C	XP_011526319.1:n.1564-277A>C
XM_005259913.2:c.2668-277A>C	XP_005259970.1:n.2668-277A>C
XM_024451518.1:c.1564-277A>C	XP_024307286.1:n.1564-277A>C
NM_000528.4:c.2665-277A>C MANE Select	NP_000519.2:n.2665-277A>C
NM_001173498.2:c.2662-277A>C	NP_001166969.1:n.2662-277A>C