Canonical Allele Identifier: CA404252925

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12774601A>G (hg19) ; chr19:g.12663787A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12663787A>G , CM000681.2:g.12663787A>G	GRCh38
NC_000019.9:g.12774601A>G , CM000681.1:g.12774601A>G	GRCh37
NC_000019.8:g.12635601A>G	NCBI36
NG_008318.1:g.7991T>C
NG_015814.1:g.1984A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000456935.7:c.679T>C MANE Select	ENSP00000395473.2:p.Trp227Arg
ENST00000221363.8:c.679T>C	ENSP00000221363.4:p.Trp227Arg
ENST00000456935.6:c.679T>C	ENSP00000395473.2:p.Trp227Arg
ENST00000466794.5:n.661T>C
ENST00000486847.2:c.382T>C	ENSP00000470174.1:p.Trp128Arg
NM_000528.3:c.679T>C	NP_000519.2:p.Trp227Arg
NM_001173498.1:c.679T>C	NP_001166969.1:p.Trp227Arg
XM_005259913.1:c.679T>C	XP_005259970.1:p.Trp227Arg
XM_005259913.2:c.679T>C	XP_005259970.1:p.Trp227Arg
XM_024451518.1:c.-340T>C	XP_024307286.1:n.-340T>C
NM_000528.4:c.679T>C MANE Select	NP_000519.2:p.Trp227Arg
NM_001173498.2:c.679T>C	NP_001166969.1:p.Trp227Arg