Canonical Allele Identifier: CA415761616
Gene: B3GALT6 HGNC NCBI

Linked Data

gnomAD v4: 1-1232635-G-A
MyVariant Identifiers: chr1:g.1168015G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1232635G>A , CM000663.2:g.1232635G>A GRCh38
NC_000001.10:g.1168015G>A , CM000663.1:g.1168015G>A GRCh37
NC_000001.9:g.1157878G>A NCBI36
NG_030007.1:g.4433C>T
NG_033265.1:g.5387G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000379198.5:c.357G>A MANE Select ENSP00000368496.2:p.Leu119=
ENST00000379198.3:c.357G>A ENSP00000368496.2:p.Leu119=
NM_080605.3:c.357G>A NP_542172.2:p.Leu119=
NM_080605.4:c.357G>A MANE Select NP_542172.2:p.Leu119=
Search 100 bp 5'
Search 100 bp 3'