Canonical Allele Identifier: CA404248551

Gene: MAN2B1

Linked Data

• dbSNP Id: rs771528526
• gnomAD v3: 19-12658437-T-G
• gnomAD v4: 19-12658437-T-G
• MyVariant Identifiers: chr19:g.12769251T>G (hg19) ; chr19:g.12658437T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12658437T>G , CM000681.2:g.12658437T>G	GRCh38
NC_000019.9:g.12769251T>G , CM000681.1:g.12769251T>G	GRCh37
NC_000019.8:g.12630251T>G	NCBI36
NG_008318.1:g.13341A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.1100A>C MANE Select	ENSP00000395473.2:p.Asn367Thr
ENST00000221363.8:c.1097A>C	ENSP00000221363.4:p.Asn366Thr
ENST00000456935.6:c.1100A>C	ENSP00000395473.2:p.Asn367Thr
ENST00000465830.1:n.181A>C
ENST00000466794.5:n.1009-93A>C
ENST00000495617.1:n.280+294A>C
NM_000528.3:c.1100A>C	NP_000519.2:p.Asn367Thr
NM_001173498.1:c.1097A>C	NP_001166969.1:p.Asn366Thr
XM_005259913.1:c.1103A>C	XP_005259970.1:p.Asn368Thr
XM_011528017.1:c.9-93A>C	XP_011526319.1:n.9-93A>C
XM_005259913.2:c.1103A>C	XP_005259970.1:p.Asn368Thr
XM_024451518.1:c.9-93A>C	XP_024307286.1:n.9-93A>C
NM_000528.4:c.1100A>C MANE Select	NP_000519.2:p.Asn367Thr
NM_001173498.2:c.1097A>C	NP_001166969.1:p.Asn366Thr