Canonical Allele Identifier: CA337824356
Gene: B3GALT6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1232593G>C , CM000663.2:g.1232593G>C GRCh38
NC_000001.10:g.1167973G>C , CM000663.1:g.1167973G>C GRCh37
NC_000001.9:g.1157836G>C NCBI36
NG_030007.1:g.4475C>G
NG_033265.1:g.5345G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000379198.5:c.315G>C MANE Select ENSP00000368496.2:p.Glu105Asp
ENST00000379198.3:c.315G>C ENSP00000368496.2:p.Glu105Asp
NM_080605.3:c.315G>C NP_542172.2:p.Glu105Asp
NM_080605.4:c.315G>C MANE Select NP_542172.2:p.Glu105Asp