Canonical Allele Identifier: CA89910073
Gene: ST6GAL1 HGNC NCBI

Linked Data

dbSNP Id: rs2239612
gnomAD v2: 3-186793242-G-A
gnomAD v3: 3-187075454-G-A
gnomAD v4: 3-187075454-G-A
MyVariant Identifiers: chr3:g.186793242G>A (hg19) chr3:g.187075454G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.187075454G>A , CM000665.2:g.187075454G>A GRCh38
NC_000003.11:g.186793242G>A , CM000665.1:g.186793242G>A GRCh37
NC_000003.10:g.188275936G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000169298.8:c.980-108G>A MANE Select ENSP00000169298.3:n.980-108G>A
ENST00000416235.6:c.980-108G>A ENSP00000414504.2:n.980-108G>A
ENST00000676633.1:c.980-108G>A ENSP00000504448.1:n.980-108G>A
ENST00000677292.1:c.980-108G>A ENSP00000503457.1:n.980-108G>A
ENST00000169298.7:c.980-108G>A ENSP00000169298.3:n.980-108G>A
ENST00000442023.1:c.287-108G>A ENSP00000403063.1:n.287-108G>A
ENST00000448044.5:c.980-108G>A ENSP00000389337.1:n.980-108G>A
ENST00000448449.1:c.765-108G>A ENSP00000415886.1:n.765-108G>A
ENST00000457772.6:c.287-108G>A ENSP00000412221.2:n.287-108G>A
ENST00000470633.1:n.1904-108G>A
NM_003032.2:c.980-108G>A NP_003023.1:n.980-108G>A
NM_173216.2:c.980-108G>A MANE Select NP_775323.1:n.980-108G>A
NM_173217.2:c.287-108G>A NP_775324.1:n.287-108G>A
XM_005247717.2:c.980-108G>A XP_005247774.1:n.980-108G>A
XM_005247719.1:c.980-108G>A XP_005247776.1:n.980-108G>A
XM_005247720.1:c.980-108G>A XP_005247777.1:n.980-108G>A
XM_006713734.1:c.980-108G>A XP_006713797.1:n.980-108G>A
XM_011513085.1:c.980-108G>A XP_011511387.1:n.980-108G>A
XM_011513086.1:c.980-108G>A XP_011511388.1:n.980-108G>A
XR_924163.1:n.1751-108G>A
NM_001353916.1:c.980-108G>A NP_001340845.1:n.980-108G>A
NM_001353916.2:c.980-108G>A NP_001340845.1:n.980-108G>A
NM_003032.3:c.980-108G>A NP_003023.1:n.980-108G>A
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