Canonical Allele Identifier: CA404243191

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12760941C>G (hg19) ; chr19:g.12650127C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12650127C>G , CM000681.2:g.12650127C>G	GRCh38
NC_000019.9:g.12760941C>G , CM000681.1:g.12760941C>G	GRCh37
NC_000019.8:g.12621941C>G	NCBI36
NG_008318.1:g.21651G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000456935.7:c.2142G>C MANE Select	ENSP00000395473.2:p.Trp714Cys
ENST00000221363.8:c.2139G>C	ENSP00000221363.4:p.Trp713Cys
ENST00000456935.6:c.2142G>C	ENSP00000395473.2:p.Trp714Cys
ENST00000466794.5:n.2732G>C
NM_000528.3:c.2142G>C	NP_000519.2:p.Trp714Cys
NM_001173498.1:c.2139G>C	NP_001166969.1:p.Trp713Cys
XM_005259913.1:c.2145G>C	XP_005259970.1:p.Trp715Cys
XM_011528017.1:c.1041G>C	XP_011526319.1:p.Trp347Cys
XM_005259913.2:c.2145G>C	XP_005259970.1:p.Trp715Cys
XM_024451518.1:c.1041G>C	XP_024307286.1:p.Trp347Cys
NM_000528.4:c.2142G>C MANE Select	NP_000519.2:p.Trp714Cys
NM_001173498.2:c.2139G>C	NP_001166969.1:p.Trp713Cys