Canonical Allele Identifier: CA415761169
Gene: B3GALT6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.1167883G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1232503G>T , CM000663.2:g.1232503G>T GRCh38
NC_000001.10:g.1167883G>T , CM000663.1:g.1167883G>T GRCh37
NC_000001.9:g.1157746G>T NCBI36
NG_030007.1:g.4565C>A
NG_033265.1:g.5255G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000379198.5:c.225G>T MANE Select ENSP00000368496.2:p.Val75=
ENST00000379198.3:c.225G>T ENSP00000368496.2:p.Val75=
NM_080605.3:c.225G>T NP_542172.2:p.Val75=
NM_080605.4:c.225G>T MANE Select NP_542172.2:p.Val75=
Search 100 bp 5'
Search 100 bp 3'