Canonical Allele Identifier: CA9226601
Gene: MAN2B1 HGNC NCBI

Linked Data

dbSNP Id: rs749826725

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12658436G>C , CM000681.2:g.12658436G>C GRCh38
NC_000019.9:g.12769250G>C , CM000681.1:g.12769250G>C GRCh37
NC_000019.8:g.12630250G>C NCBI36
NG_008318.1:g.13342C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000456935.7:c.1101C>G MANE Select ENSP00000395473.2:p.Asn367Lys
ENST00000221363.8:c.1098C>G ENSP00000221363.4:p.Asn366Lys
ENST00000456935.6:c.1101C>G ENSP00000395473.2:p.Asn367Lys
ENST00000465830.1:n.182C>G
ENST00000466794.5:n.1009-92C>G
ENST00000495617.1:n.280+295C>G
NM_000528.3:c.1101C>G NP_000519.2:p.Asn367Lys
NM_001173498.1:c.1098C>G NP_001166969.1:p.Asn366Lys
XM_005259913.1:c.1104C>G XP_005259970.1:p.Asn368Lys
XM_011528017.1:c.9-92C>G XP_011526319.1:n.9-92C>G
XM_005259913.2:c.1104C>G XP_005259970.1:p.Asn368Lys
XM_024451518.1:c.9-92C>G XP_024307286.1:n.9-92C>G
NM_000528.4:c.1101C>G MANE Select NP_000519.2:p.Asn367Lys
NM_001173498.2:c.1098C>G NP_001166969.1:p.Asn366Lys