Canonical Allele Identifier: CA404243577

Gene: MAN2B1

Linked Data

• MyVariant Identifiers: chr19:g.12761013G>C (hg19) ; chr19:g.12650199G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12650199G>C , CM000681.2:g.12650199G>C	GRCh38
NC_000019.9:g.12761013G>C , CM000681.1:g.12761013G>C	GRCh37
NC_000019.8:g.12622013G>C	NCBI36
NG_008318.1:g.21579C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000456935.7:c.2070C>G MANE Select	ENSP00000395473.2:p.His690Gln
ENST00000221363.8:c.2067C>G	ENSP00000221363.4:p.His689Gln
ENST00000456935.6:c.2070C>G	ENSP00000395473.2:p.His690Gln
ENST00000466794.5:n.2660C>G
NM_000528.3:c.2070C>G	NP_000519.2:p.His690Gln
NM_001173498.1:c.2067C>G	NP_001166969.1:p.His689Gln
XM_005259913.1:c.2073C>G	XP_005259970.1:p.His691Gln
XM_011528017.1:c.969C>G	XP_011526319.1:p.His323Gln
XM_005259913.2:c.2073C>G	XP_005259970.1:p.His691Gln
XM_024451518.1:c.969C>G	XP_024307286.1:p.His323Gln
NM_000528.4:c.2070C>G MANE Select	NP_000519.2:p.His690Gln
NM_001173498.2:c.2067C>G	NP_001166969.1:p.His689Gln