Canonical Allele Identifier: CA404255788

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12776169G>C (hg19) ; chr19:g.12665355G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12665355G>C , CM000681.2:g.12665355G>C	GRCh38
NC_000019.9:g.12776169G>C , CM000681.1:g.12776169G>C	GRCh37
NC_000019.8:g.12637169G>C	NCBI36
NG_008318.1:g.6423C>G
NG_015814.1:g.3552G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.433C>G MANE Select	ENSP00000395473.2:p.Gln145Glu
ENST00000221363.8:c.433C>G	ENSP00000221363.4:p.Gln145Glu
ENST00000456935.6:c.433C>G	ENSP00000395473.2:p.Gln145Glu
ENST00000466794.5:n.415C>G
ENST00000486847.2:c.330C>G	ENSP00000470174.1:p.Ala110=
ENST00000596512.5:n.371C>G
ENST00000597961.1:c.424C>G	ENSP00000472710.1:p.Gln142Glu
ENST00000598876.1:c.460C>G	ENSP00000470533.1:p.Gln154Glu
ENST00000600281.1:n.474C>G
NM_000528.3:c.433C>G	NP_000519.2:p.Gln145Glu
NM_001173498.1:c.433C>G	NP_001166969.1:p.Gln145Glu
XM_005259913.1:c.433C>G	XP_005259970.1:p.Gln145Glu
XM_005259913.2:c.433C>G	XP_005259970.1:p.Gln145Glu
XM_024451518.1:c.-586C>G	XP_024307286.1:n.-586C>G
NM_000528.4:c.433C>G MANE Select	NP_000519.2:p.Gln145Glu
NM_001173498.2:c.433C>G	NP_001166969.1:p.Gln145Glu