Canonical Allele Identifier: CA404247839

Gene: MAN2B1

Linked Data

• dbSNP Id: rs1302481119
• gnomAD v2: 19-12769055-T-C
• gnomAD v3: 19-12658241-T-C
• gnomAD v4: 19-12658241-T-C
• MyVariant Identifiers: chr19:g.12769055T>C (hg19) ; chr19:g.12658241T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12658241T>C , CM000681.2:g.12658241T>C	GRCh38
NC_000019.9:g.12769055T>C , CM000681.1:g.12769055T>C	GRCh37
NC_000019.8:g.12630055T>C	NCBI36
NG_008318.1:g.13537A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.1213A>G MANE Select	ENSP00000395473.2:p.Ser405Gly
ENST00000221363.8:c.1210A>G	ENSP00000221363.4:p.Ser404Gly
ENST00000456935.6:c.1213A>G	ENSP00000395473.2:p.Ser405Gly
ENST00000465830.1:n.377A>G
ENST00000466794.5:n.1112A>G
ENST00000495617.1:n.281-481A>G
NM_000528.3:c.1213A>G	NP_000519.2:p.Ser405Gly
NM_001173498.1:c.1210A>G	NP_001166969.1:p.Ser404Gly
XM_005259913.1:c.1216A>G	XP_005259970.1:p.Ser406Gly
XM_011528017.1:c.112A>G	XP_011526319.1:p.Ser38Gly
XM_005259913.2:c.1216A>G	XP_005259970.1:p.Ser406Gly
XM_024451518.1:c.112A>G	XP_024307286.1:p.Ser38Gly
NM_000528.4:c.1213A>G MANE Select	NP_000519.2:p.Ser405Gly
NM_001173498.2:c.1210A>G	NP_001166969.1:p.Ser404Gly