Canonical Allele Identifier: CA404258096

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12776550A>T (hg19) ; chr19:g.12665736A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12665736A>T , CM000681.2:g.12665736A>T	GRCh38
NC_000019.9:g.12776550A>T , CM000681.1:g.12776550A>T	GRCh37
NC_000019.8:g.12637550A>T	NCBI36
NG_008318.1:g.6042T>A
NG_015814.1:g.3933A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.229T>A MANE Select	ENSP00000395473.2:p.Trp77Arg
ENST00000221363.8:c.229T>A	ENSP00000221363.4:p.Trp77Arg
ENST00000456935.6:c.229T>A	ENSP00000395473.2:p.Trp77Arg
ENST00000466794.5:n.211T>A
ENST00000486847.2:c.160-211T>A	ENSP00000470174.1:n.160-211T>A
ENST00000596512.5:n.201-211T>A
ENST00000597961.1:c.220T>A	ENSP00000472710.1:p.Trp74Arg
ENST00000598876.1:c.256T>A	ENSP00000470533.1:p.Trp86Arg
ENST00000600281.1:n.270T>A
NM_000528.3:c.229T>A	NP_000519.2:p.Trp77Arg
NM_001173498.1:c.229T>A	NP_001166969.1:p.Trp77Arg
XM_005259913.1:c.229T>A	XP_005259970.1:p.Trp77Arg
XM_005259913.2:c.229T>A	XP_005259970.1:p.Trp77Arg
XM_024451518.1:c.-790T>A	XP_024307286.1:n.-790T>A
NM_000528.4:c.229T>A MANE Select	NP_000519.2:p.Trp77Arg
NM_001173498.2:c.229T>A	NP_001166969.1:p.Trp77Arg