Canonical Allele Identifier: CA404238019

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12758352C>G (hg19) ; chr19:g.12647538C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12647538C>G , CM000681.2:g.12647538C>G	GRCh38
NC_000019.9:g.12758352C>G , CM000681.1:g.12758352C>G	GRCh37
NC_000019.8:g.12619352C>G	NCBI36
NG_008318.1:g.24240G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.2725G>C MANE Select	ENSP00000395473.2:p.Gly909Arg
ENST00000221363.8:c.2722G>C	ENSP00000221363.4:p.Gly908Arg
ENST00000456935.6:c.2725G>C	ENSP00000395473.2:p.Gly909Arg
ENST00000466794.5:n.3315G>C
ENST00000469423.1:n.47G>C
ENST00000493218.5:n.136G>C
ENST00000597692.1:c.284G>C
NM_000528.3:c.2725G>C	NP_000519.2:p.Gly909Arg
NM_001173498.1:c.2722G>C	NP_001166969.1:p.Gly908Arg
XM_005259913.1:c.2728G>C	XP_005259970.1:p.Gly910Arg
XM_011528017.1:c.1624G>C	XP_011526319.1:p.Gly542Arg
XM_005259913.2:c.2728G>C	XP_005259970.1:p.Gly910Arg
XM_024451518.1:c.1624G>C	XP_024307286.1:p.Gly542Arg
NM_000528.4:c.2725G>C MANE Select	NP_000519.2:p.Gly909Arg
NM_001173498.2:c.2722G>C	NP_001166969.1:p.Gly908Arg