Canonical Allele Identifier: CA2622576147
Gene: B3GLCT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.31317684_31317689dup , CM000675.2:g.31317684_31317689dup GRCh38
NC_000013.10:g.31891821_31891826dup , CM000675.1:g.31891821_31891826dup GRCh37
NC_000013.9:g.30789821_30789826dup NCBI36
NG_011732.1:g.122710_122715dup
NG_011732.2:g.122710_122715dup

Transcript Alleles

HGVS Amino-acid change
ENST00000343307.5:c.1183_1184+4dup
ENST00000343307.4:c.1183_1184+4dup
NM_194318.3:c.1183_1184+4dup
XM_006719768.2:c.1126_1127+4dup
XM_011534936.1:c.1065-6067_1065-6062dup XP_011533238.1:n.1065-6067_1065-6062dup
XM_011534937.1:c.1063_1064+4dup
XM_011534938.1:c.1036_1037+4dup
XM_006719768.3:c.1126_1127+4dup
XM_011534938.2:c.1036_1037+4dup
XM_017020395.1:c.1036_1037+4dup
NM_194318.4:c.1183_1184+4dup