Canonical Allele Identifier: CA505770574

Gene: MAN2B1

Linked Data

• dbSNP Id: rs142797984
• MyVariant Identifiers: chr19:g.12758084G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12647270G>C , CM000681.2:g.12647270G>C	GRCh38
NC_000019.9:g.12758084G>C , CM000681.1:g.12758084G>C	GRCh37
NC_000019.8:g.12619084G>C	NCBI36
NG_008318.1:g.24508C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.2886C>G MANE Select	ENSP00000395473.2:p.Arg962=
ENST00000221363.8:c.2883C>G	ENSP00000221363.4:p.Arg961=
ENST00000456935.6:c.2886C>G	ENSP00000395473.2:p.Arg962=
ENST00000466794.5:n.3476C>G
ENST00000469423.1:n.315C>G
ENST00000493218.5:n.297C>G
ENST00000597692.1:c.445C>G
NM_000528.3:c.2886C>G	NP_000519.2:p.Arg962=
NM_001173498.1:c.2883C>G	NP_001166969.1:p.Arg961=
XM_005259913.1:c.2889C>G	XP_005259970.1:p.Arg963=
XM_011528017.1:c.1785C>G	XP_011526319.1:p.Arg595=
XM_005259913.2:c.2889C>G	XP_005259970.1:p.Arg963=
XM_024451518.1:c.1785C>G	XP_024307286.1:p.Arg595=
NM_000528.4:c.2886C>G MANE Select	NP_000519.2:p.Arg962=
NM_001173498.2:c.2883C>G	NP_001166969.1:p.Arg961=