Canonical Allele Identifier: CA404237813

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12758303T>G (hg19) ; chr19:g.12647489T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12647489T>G , CM000681.2:g.12647489T>G	GRCh38
NC_000019.9:g.12758303T>G , CM000681.1:g.12758303T>G	GRCh37
NC_000019.8:g.12619303T>G	NCBI36
NG_008318.1:g.24289A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000456935.7:c.2774A>C MANE Select	ENSP00000395473.2:p.Glu925Ala
ENST00000221363.8:c.2771A>C	ENSP00000221363.4:p.Glu924Ala
ENST00000456935.6:c.2774A>C	ENSP00000395473.2:p.Glu925Ala
ENST00000466794.5:n.3364A>C
ENST00000469423.1:n.96A>C
ENST00000493218.5:n.185A>C
ENST00000597692.1:c.333A>C
NM_000528.3:c.2774A>C	NP_000519.2:p.Glu925Ala
NM_001173498.1:c.2771A>C	NP_001166969.1:p.Glu924Ala
XM_005259913.1:c.2777A>C	XP_005259970.1:p.Glu926Ala
XM_011528017.1:c.1673A>C	XP_011526319.1:p.Glu558Ala
XM_005259913.2:c.2777A>C	XP_005259970.1:p.Glu926Ala
XM_024451518.1:c.1673A>C	XP_024307286.1:p.Glu558Ala
NM_000528.4:c.2774A>C MANE Select	NP_000519.2:p.Glu925Ala
NM_001173498.2:c.2771A>C	NP_001166969.1:p.Glu924Ala