Canonical Allele Identifier: CA404255932

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12776182T>G (hg19) ; chr19:g.12665368T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12665368T>G , CM000681.2:g.12665368T>G	GRCh38
NC_000019.9:g.12776182T>G , CM000681.1:g.12776182T>G	GRCh37
NC_000019.8:g.12637182T>G	NCBI36
NG_008318.1:g.6410A>C
NG_015814.1:g.3565T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.420A>C MANE Select	ENSP00000395473.2:p.Arg140=
ENST00000221363.8:c.420A>C	ENSP00000221363.4:p.Arg140=
ENST00000456935.6:c.420A>C	ENSP00000395473.2:p.Arg140=
ENST00000466794.5:n.402A>C
ENST00000486847.2:c.317A>C	ENSP00000470174.1:p.Glu106Ala
ENST00000596512.5:n.358A>C
ENST00000597961.1:c.411A>C	ENSP00000472710.1:p.Arg137=
ENST00000598876.1:c.447A>C	ENSP00000470533.1:p.Arg149=
ENST00000600281.1:n.461A>C
NM_000528.3:c.420A>C	NP_000519.2:p.Arg140=
NM_001173498.1:c.420A>C	NP_001166969.1:p.Arg140=
XM_005259913.1:c.420A>C	XP_005259970.1:p.Arg140=
XM_005259913.2:c.420A>C	XP_005259970.1:p.Arg140=
XM_024451518.1:c.-599A>C	XP_024307286.1:n.-599A>C
NM_000528.4:c.420A>C MANE Select	NP_000519.2:p.Arg140=
NM_001173498.2:c.420A>C	NP_001166969.1:p.Arg140=