Canonical Allele Identifier: CA404241299

Gene: MAN2B1

Linked Data

• dbSNP Id: rs2023775839
• gnomAD v3: 19-12649206-A-C
• gnomAD v4: 19-12649206-A-C
• MyVariant Identifiers: chr19:g.12760020A>C (hg19) ; chr19:g.12649206A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12649206A>C , CM000681.2:g.12649206A>C	GRCh38
NC_000019.9:g.12760020A>C , CM000681.1:g.12760020A>C	GRCh37
NC_000019.8:g.12621020A>C	NCBI36
NG_008318.1:g.22572T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.2366T>G MANE Select	ENSP00000395473.2:p.Met789Arg
ENST00000221363.8:c.2363T>G	ENSP00000221363.4:p.Met788Arg
ENST00000456935.6:c.2366T>G	ENSP00000395473.2:p.Met789Arg
ENST00000466794.5:n.2956T>G
NM_000528.3:c.2366T>G	NP_000519.2:p.Met789Arg
NM_001173498.1:c.2363T>G	NP_001166969.1:p.Met788Arg
XM_005259913.1:c.2369T>G	XP_005259970.1:p.Met790Arg
XM_011528017.1:c.1265T>G	XP_011526319.1:p.Met422Arg
XM_005259913.2:c.2369T>G	XP_005259970.1:p.Met790Arg
XM_024451518.1:c.1265T>G	XP_024307286.1:p.Met422Arg
NM_000528.4:c.2366T>G MANE Select	NP_000519.2:p.Met789Arg
NM_001173498.2:c.2363T>G	NP_001166969.1:p.Met788Arg