Canonical Allele Identifier: CA404258170

Gene: MAN2B1

Linked Data

• dbSNP Id: rs2145290683
• gnomAD v3: 19-12665745-C-T
• gnomAD v4: 19-12665745-C-T
• MyVariant Identifiers: chr19:g.12776559C>T (hg19) ; chr19:g.12665745C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12665745C>T , CM000681.2:g.12665745C>T	GRCh38
NC_000019.9:g.12776559C>T , CM000681.1:g.12776559C>T	GRCh37
NC_000019.8:g.12637559C>T	NCBI36
NG_008318.1:g.6033G>A
NG_015814.1:g.3942C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000456935.7:c.220G>A MANE Select	ENSP00000395473.2:p.Asp74Asn
ENST00000221363.8:c.220G>A	ENSP00000221363.4:p.Asp74Asn
ENST00000456935.6:c.220G>A	ENSP00000395473.2:p.Asp74Asn
ENST00000466794.5:n.202G>A
ENST00000486847.2:c.160-220G>A	ENSP00000470174.1:n.160-220G>A
ENST00000596512.5:n.201-220G>A
ENST00000597961.1:c.211G>A	ENSP00000472710.1:p.Asp71Asn
ENST00000598876.1:c.247G>A	ENSP00000470533.1:p.Asp83Asn
ENST00000600281.1:n.261G>A
NM_000528.3:c.220G>A	NP_000519.2:p.Asp74Asn
NM_001173498.1:c.220G>A	NP_001166969.1:p.Asp74Asn
XM_005259913.1:c.220G>A	XP_005259970.1:p.Asp74Asn
XM_005259913.2:c.220G>A	XP_005259970.1:p.Asp74Asn
XM_024451518.1:c.-799G>A	XP_024307286.1:n.-799G>A
NM_000528.4:c.220G>A MANE Select	NP_000519.2:p.Asp74Asn
NM_001173498.2:c.220G>A	NP_001166969.1:p.Asp74Asn