Canonical Allele Identifier: CA404241306

Gene: MAN2B1

Linked Data

• gnomAD v4: 19-12649207-T-C
• MyVariant Identifiers: chr19:g.12760021T>C (hg19) ; chr19:g.12649207T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12649207T>C , CM000681.2:g.12649207T>C	GRCh38
NC_000019.9:g.12760021T>C , CM000681.1:g.12760021T>C	GRCh37
NC_000019.8:g.12621021T>C	NCBI36
NG_008318.1:g.22571A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.2365A>G MANE Select	ENSP00000395473.2:p.Met789Val
ENST00000221363.8:c.2362A>G	ENSP00000221363.4:p.Met788Val
ENST00000456935.6:c.2365A>G	ENSP00000395473.2:p.Met789Val
ENST00000466794.5:n.2955A>G
NM_000528.3:c.2365A>G	NP_000519.2:p.Met789Val
NM_001173498.1:c.2362A>G	NP_001166969.1:p.Met788Val
XM_005259913.1:c.2368A>G	XP_005259970.1:p.Met790Val
XM_011528017.1:c.1264A>G	XP_011526319.1:p.Met422Val
XM_005259913.2:c.2368A>G	XP_005259970.1:p.Met790Val
XM_024451518.1:c.1264A>G	XP_024307286.1:p.Met422Val
NM_000528.4:c.2365A>G MANE Select	NP_000519.2:p.Met789Val
NM_001173498.2:c.2362A>G	NP_001166969.1:p.Met788Val