Canonical Allele Identifier: CA505770880

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12768899G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12658085G>C , CM000681.2:g.12658085G>C	GRCh38
NC_000019.9:g.12768899G>C , CM000681.1:g.12768899G>C	GRCh37
NC_000019.8:g.12629899G>C	NCBI36
NG_008318.1:g.13693C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.1287C>G MANE Select	ENSP00000395473.2:p.Gly429=
ENST00000221363.8:c.1284C>G	ENSP00000221363.4:p.Gly428=
ENST00000456935.6:c.1287C>G	ENSP00000395473.2:p.Gly429=
ENST00000465830.1:n.451C>G
ENST00000466794.5:n.1186C>G
ENST00000495617.1:n.281-325C>G
NM_000528.3:c.1287C>G	NP_000519.2:p.Gly429=
NM_001173498.1:c.1284C>G	NP_001166969.1:p.Gly428=
XM_005259913.1:c.1290C>G	XP_005259970.1:p.Gly430=
XM_011528017.1:c.186C>G	XP_011526319.1:p.Gly62=
XM_005259913.2:c.1290C>G	XP_005259970.1:p.Gly430=
XM_024451518.1:c.186C>G	XP_024307286.1:p.Gly62=
NM_000528.4:c.1287C>G MANE Select	NP_000519.2:p.Gly429=
NM_001173498.2:c.1284C>G	NP_001166969.1:p.Gly428=