Canonical Allele Identifier: CA9226921

Gene: MAN2B1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12666683C>G , CM000681.2:g.12666683C>G	GRCh38
NC_000019.9:g.12777497C>G , CM000681.1:g.12777497C>G	GRCh37
NC_000019.8:g.12638497C>G	NCBI36
NG_008318.1:g.5095G>C
NG_015814.1:g.4880C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000528.4:c.19G>C MANE Select	NP_000519.2:p.Ala7Pro
ENST00000456935.7:c.19G>C MANE Select	ENSP00000395473.2:p.Ala7Pro
NM_000528.3:c.19G>C	NP_000519.2:p.Ala7Pro
NM_001173498.1:c.19G>C	NP_001166969.1:p.Ala7Pro
NM_001173498.2:c.19G>C	NP_001166969.1:p.Ala7Pro
ENST00000221363.8:c.19G>C	ENSP00000221363.4:p.Ala7Pro
ENST00000456935.6:c.19G>C	ENSP00000395473.2:p.Ala7Pro
ENST00000466794.5:n.1G>C
ENST00000486847.2:c.19G>C	ENSP00000470174.1:p.Ala7Pro
ENST00000596512.5:n.60G>C
ENST00000597961.1:c.151-878G>C	ENSP00000472710.1:n.151-878G>C
ENST00000598876.1:c.19G>C	ENSP00000470533.1:p.Ala7Pro
ENST00000600281.1:n.60G>C
XM_005259913.1:c.19G>C	XP_005259970.1:p.Ala7Pro
XM_005259913.2:c.19G>C	XP_005259970.1:p.Ala7Pro
XM_024451518.1:c.-1000G>C	XP_024307286.1:n.-1000G>C