Canonical Allele Identifier: CA404256751

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12776260A>G (hg19) ; chr19:g.12665446A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12665446A>G , CM000681.2:g.12665446A>G	GRCh38
NC_000019.9:g.12776260A>G , CM000681.1:g.12776260A>G	GRCh37
NC_000019.8:g.12637260A>G	NCBI36
NG_008318.1:g.6332T>C
NG_015814.1:g.3643A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.342T>C MANE Select	ENSP00000395473.2:p.Arg114=
ENST00000221363.8:c.342T>C	ENSP00000221363.4:p.Arg114=
ENST00000456935.6:c.342T>C	ENSP00000395473.2:p.Arg114=
ENST00000466794.5:n.324T>C
ENST00000486847.2:c.239T>C	ENSP00000470174.1:p.Val80Ala
ENST00000596512.5:n.280T>C
ENST00000597961.1:c.333T>C	ENSP00000472710.1:p.Arg111=
ENST00000598876.1:c.369T>C	ENSP00000470533.1:p.Arg123=
ENST00000600281.1:n.383T>C
NM_000528.3:c.342T>C	NP_000519.2:p.Arg114=
NM_001173498.1:c.342T>C	NP_001166969.1:p.Arg114=
XM_005259913.1:c.342T>C	XP_005259970.1:p.Arg114=
XM_005259913.2:c.342T>C	XP_005259970.1:p.Arg114=
XM_024451518.1:c.-677T>C	XP_024307286.1:n.-677T>C
NM_000528.4:c.342T>C MANE Select	NP_000519.2:p.Arg114=
NM_001173498.2:c.342T>C	NP_001166969.1:p.Arg114=