Canonical Allele Identifier: CA337823570
Gene: B3GALT6 HGNC NCBI

Linked Data

gnomAD v4: 1-1232511-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1232511G>A , CM000663.2:g.1232511G>A GRCh38
NC_000001.10:g.1167891G>A , CM000663.1:g.1167891G>A GRCh37
NC_000001.9:g.1157754G>A NCBI36
NG_030007.1:g.4557C>T
NG_033265.1:g.5263G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000379198.5:c.233G>A MANE Select ENSP00000368496.2:p.Ser78Asn
ENST00000379198.3:c.233G>A ENSP00000368496.2:p.Ser78Asn
NM_080605.3:c.233G>A NP_542172.2:p.Ser78Asn
NM_080605.4:c.233G>A MANE Select NP_542172.2:p.Ser78Asn