Canonical Allele Identifier: CA404246122

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12767774T>A (hg19) ; chr19:g.12656960T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12656960T>A , CM000681.2:g.12656960T>A	GRCh38
NC_000019.9:g.12767774T>A , CM000681.1:g.12767774T>A	GRCh37
NC_000019.8:g.12628774T>A	NCBI36
NG_008318.1:g.14818A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.1516A>T MANE Select	ENSP00000395473.2:p.Thr506Ser
ENST00000221363.8:c.1513A>T	ENSP00000221363.4:p.Thr505Ser
ENST00000433513.5:n.122A>T
ENST00000456935.6:c.1516A>T	ENSP00000395473.2:p.Thr506Ser
ENST00000466794.5:n.1415A>T
ENST00000495617.1:n.692A>T
ENST00000593686.1:c.126A>T
ENST00000595880.5:n.113A>T
NM_000528.3:c.1516A>T	NP_000519.2:p.Thr506Ser
NM_001173498.1:c.1513A>T	NP_001166969.1:p.Thr505Ser
XM_005259913.1:c.1519A>T	XP_005259970.1:p.Thr507Ser
XM_011528017.1:c.415A>T	XP_011526319.1:p.Thr139Ser
XM_005259913.2:c.1519A>T	XP_005259970.1:p.Thr507Ser
XM_024451518.1:c.415A>T	XP_024307286.1:p.Thr139Ser
NM_000528.4:c.1516A>T MANE Select	NP_000519.2:p.Thr506Ser
NM_001173498.2:c.1513A>T	NP_001166969.1:p.Thr505Ser