Canonical Allele Identifier: CA505625464

Gene: MAN2B1

Linked Data

• gnomAD v4: 19-12663394-G-A
• MyVariant Identifiers: chr19:g.12774208G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12663394G>A , CM000681.2:g.12663394G>A	GRCh38
NC_000019.9:g.12774208G>A , CM000681.1:g.12774208G>A	GRCh37
NC_000019.8:g.12635208G>A	NCBI36
NG_008318.1:g.8384C>T
NG_015814.1:g.1591G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000456935.7:c.832C>T MANE Select	ENSP00000395473.2:p.Leu278=
ENST00000221363.8:c.832C>T	ENSP00000221363.4:p.Leu278=
ENST00000456935.6:c.832C>T	ENSP00000395473.2:p.Leu278=
ENST00000462144.1:n.25C>T
ENST00000466794.5:n.814C>T
NM_000528.3:c.832C>T	NP_000519.2:p.Leu278=
NM_001173498.1:c.832C>T	NP_001166969.1:p.Leu278=
XM_005259913.1:c.832C>T	XP_005259970.1:p.Leu278=
XM_005259913.2:c.832C>T	XP_005259970.1:p.Leu278=
XM_024451518.1:c.-187C>T	XP_024307286.1:n.-187C>T
NM_000528.4:c.832C>T MANE Select	NP_000519.2:p.Leu278=
NM_001173498.2:c.832C>T	NP_001166969.1:p.Leu278=