Canonical Allele Identifier: CA404237574

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12758148T>G (hg19) ; chr19:g.12647334T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12647334T>G , CM000681.2:g.12647334T>G	GRCh38
NC_000019.9:g.12758148T>G , CM000681.1:g.12758148T>G	GRCh37
NC_000019.8:g.12619148T>G	NCBI36
NG_008318.1:g.24444A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.2822A>C MANE Select	ENSP00000395473.2:p.Asp941Ala
ENST00000221363.8:c.2819A>C	ENSP00000221363.4:p.Asp940Ala
ENST00000456935.6:c.2822A>C	ENSP00000395473.2:p.Asp941Ala
ENST00000466794.5:n.3412A>C
ENST00000469423.1:n.251A>C
ENST00000493218.5:n.233A>C
ENST00000597692.1:c.381A>C
NM_000528.3:c.2822A>C	NP_000519.2:p.Asp941Ala
NM_001173498.1:c.2819A>C	NP_001166969.1:p.Asp940Ala
XM_005259913.1:c.2825A>C	XP_005259970.1:p.Asp942Ala
XM_011528017.1:c.1721A>C	XP_011526319.1:p.Asp574Ala
XM_005259913.2:c.2825A>C	XP_005259970.1:p.Asp942Ala
XM_024451518.1:c.1721A>C	XP_024307286.1:p.Asp574Ala
NM_000528.4:c.2822A>C MANE Select	NP_000519.2:p.Asp941Ala
NM_001173498.2:c.2819A>C	NP_001166969.1:p.Asp940Ala