Canonical Allele Identifier: CA783350233

Gene: MAN2B1

Linked Data

• dbSNP Id: rs1366309883
• gnomAD v3: 19-12658641-C-G
• gnomAD v4: 19-12658641-C-G
• MyVariant Identifiers: chr19:g.12769455C>G (hg19) ; chr19:g.12658641C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12658641C>G , CM000681.2:g.12658641C>G	GRCh38
NC_000019.9:g.12769455C>G , CM000681.1:g.12769455C>G	GRCh37
NC_000019.8:g.12630455C>G	NCBI36
NG_008318.1:g.13137G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.1027-131G>C MANE Select	ENSP00000395473.2:n.1027-131G>C
ENST00000221363.8:c.1027-134G>C	ENSP00000221363.4:n.1027-134G>C
ENST00000456935.6:c.1027-131G>C	ENSP00000395473.2:n.1027-131G>C
ENST00000466794.5:n.1009-297G>C
ENST00000495617.1:n.280+90G>C
NM_000528.3:c.1027-131G>C	NP_000519.2:n.1027-131G>C
NM_001173498.1:c.1027-134G>C	NP_001166969.1:n.1027-134G>C
XM_005259913.1:c.1027-128G>C	XP_005259970.1:n.1027-128G>C
XM_011528017.1:c.9-297G>C	XP_011526319.1:n.9-297G>C
XM_005259913.2:c.1027-128G>C	XP_005259970.1:n.1027-128G>C
XM_024451518.1:c.9-297G>C	XP_024307286.1:n.9-297G>C
NM_000528.4:c.1027-131G>C MANE Select	NP_000519.2:n.1027-131G>C
NM_001173498.2:c.1027-134G>C	NP_001166969.1:n.1027-134G>C