Canonical Allele Identifier: CA2748218313

Gene: B3GALNT2 TBCE

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.235450361C>G , CM000663.2:g.235450361C>G	GRCh38
NC_000001.10:g.235613676C>G , CM000663.1:g.235613676C>G	GRCh37
NC_000001.9:g.233680299C>G	NCBI36
NG_009230.1:g.87949C>G
NG_033219.2:g.59121G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366600.8:c.1369-21G>C (B3GALNT2) MANE Select	ENSP00000355559.3:n.1369-21G>C
ENST00000642610.2:c.*1599C>G (TBCE) MANE Select	ENSP00000494796.1:n.*1599C>G
ENST00000675193.1:c.*309-21G>C (B3GALNT2)	ENSP00000502069.1:n.*309-21G>C
ENST00000675555.1:c.1147-21G>C (B3GALNT2)	ENSP00000501896.1:n.1147-21G>C
ENST00000676288.1:c.*996G>C (B3GALNT2)	ENSP00000502392.1:n.*996G>C
ENST00000366600.7:c.1369-21G>C (B3GALNT2)	ENSP00000355559.3:n.1369-21G>C
NM_152490.4:c.1369-21G>C (B3GALNT2)	NP_689703.1:n.1369-21G>C
XM_006711749.2:c.1369-21G>C (B3GALNT2)	XP_006711812.1:n.1369-21G>C
XM_006711749.3:c.1369-21G>C (B3GALNT2)	XP_006711812.1:n.1369-21G>C
XM_017000394.1:c.1492-21G>C (B3GALNT2)	XP_016855883.1:n.1492-21G>C
XM_017000395.1:c.*45-21G>C (B3GALNT2)	XP_016855884.1:n.*45-21G>C
XR_001736987.1:n.1473-21G>C (B3GALNT2)
XR_001736989.1:n.1394-21G>C (B3GALNT2)
XR_001736990.1:n.1356-21G>C (B3GALNT2)
NM_003193.5:c.*1599C>G (TBCE) MANE Select	NP_003184.1:n.*1599C>G
NM_152490.5:c.1369-21G>C (B3GALNT2) MANE Select	NP_689703.1:n.1369-21G>C
NM_001079515.3:c.*1599C>G (TBCE)	NP_001072983.1:n.*1599C>G
NM_001287801.2:c.*1599C>G (TBCE)	NP_001274730.1:n.*1599C>G
NM_001287802.2:c.*1599C>G (TBCE)	NP_001274731.1:n.*1599C>G