Canonical Allele Identifier: CA2486521405
Gene: B3GALNT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.235489231C= , CM000663.2:g.235489231C= GRCh38
NC_000001.10:g.235652536C= , CM000663.1:g.235652536C= GRCh37
NC_000001.9:g.233719159C= NCBI36
NG_033219.2:g.20251G=

Transcript Alleles

HGVS Amino-acid change
ENST00000366600.8:c.298G= MANE Select ENSP00000355559.3:p.Glu100=
ENST00000675193.1:c.421G= ENSP00000502069.1:p.Glu141=
ENST00000675555.1:c.76G= ENSP00000501896.1:p.Glu26=
ENST00000676288.1:c.421G= ENSP00000502392.1:p.Glu141=
ENST00000313984.3:c.421G= ENSP00000315678.3:p.Glu141=
ENST00000366600.7:c.298G= ENSP00000355559.3:p.Glu100=
ENST00000494378.1:n.434-4716G=
ENST00000612859.4:c.261-4716G= ENSP00000481548.1:n.261-4716G=
NM_001277155.2:c.421G= NP_001264084.1:p.Glu141=
NM_152490.4:c.298G= NP_689703.1:p.Glu100=
XM_005273071.3:c.298G= XP_005273128.1:p.Glu100=
XM_006711749.2:c.298G= XP_006711812.1:p.Glu100=
XM_011544096.1:c.298G= XP_011542398.1:p.Glu100=
XM_011544097.1:c.298G= XP_011542399.1:p.Glu100=
XM_006711749.3:c.298G= XP_006711812.1:p.Glu100=
XM_017000394.1:c.421G= XP_016855883.1:p.Glu141=
XM_017000395.1:c.421G= XP_016855884.1:p.Glu141=
XR_001736987.1:n.586G=
XR_001736988.1:n.586G=
XR_001736989.1:n.586G=
XR_001736990.1:n.469G=
NM_152490.5:c.298G= MANE Select NP_689703.1:p.Glu100=
NM_001277155.3:c.421G= NP_001264084.1:p.Glu141=