Canonical Allele Identifier: CA738887739

Gene: ST6GALNAC3

Linked Data

• dbSNP Id: rs1247673179
• gnomAD v3: 1-76226892-T-C
• gnomAD v4: 1-76226892-T-C
• MyVariant Identifiers: chr1:g.76692577T>C (hg19) ; chr1:g.76226892T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.76226892T>C , CM000663.2:g.76226892T>C	GRCh38
NC_000001.10:g.76692577T>C , CM000663.1:g.76692577T>C	GRCh37
NC_000001.9:g.76465165T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328299.4:c.19-86913T>C MANE Select	ENSP00000329214.3:n.19-86913T>C
ENST00000328299.3:c.19-86913T>C	ENSP00000329214.3:n.19-86913T>C
NM_001160011.1:c.19-86913T>C	NP_001153483.1:n.19-86913T>C
NM_152996.2:c.19-86913T>C	NP_694541.2:n.19-86913T>C
XM_006710553.2:c.-53-82614T>C	XP_006710616.1:n.-53-82614T>C
NM_001160011.2:c.19-86913T>C	NP_001153483.1:n.19-86913T>C
NM_001349105.1:c.18+152008T>C	NP_001336034.1:n.18+152008T>C
NM_001349106.1:c.-485-82614T>C	NP_001336035.1:n.-485-82614T>C
NM_001349107.1:c.19-86913T>C	NP_001336036.1:n.19-86913T>C
NM_001349108.1:c.18+152008T>C	NP_001336037.1:n.18+152008T>C
NM_001349109.1:c.19-86913T>C	NP_001336038.1:n.19-86913T>C
NM_001349110.1:c.19-86913T>C	NP_001336039.1:n.19-86913T>C
NM_001349111.1:c.-53-82614T>C	NP_001336040.1:n.-53-82614T>C
NM_152996.3:c.19-86913T>C	NP_694541.2:n.19-86913T>C
NR_146056.1:n.202-86913T>C
XR_001737094.2:n.152-86913T>C
NM_152996.4:c.19-86913T>C MANE Select	NP_694541.2:n.19-86913T>C
NM_001160011.3:c.19-86913T>C	NP_001153483.1:n.19-86913T>C
NM_001349105.2:c.18+152008T>C	NP_001336034.1:n.18+152008T>C
NM_001349106.2:c.-485-82614T>C	NP_001336035.1:n.-485-82614T>C
NM_001349107.2:c.19-86913T>C	NP_001336036.1:n.19-86913T>C
NM_001349108.2:c.18+152008T>C	NP_001336037.1:n.18+152008T>C
NM_001349109.2:c.19-86913T>C	NP_001336038.1:n.19-86913T>C
NM_001349110.2:c.19-86913T>C	NP_001336039.1:n.19-86913T>C
NM_001349111.2:c.-53-82614T>C	NP_001336040.1:n.-53-82614T>C
NR_146056.2:n.140-86913T>C
NM_001349109.3:c.19-86913T>C	NP_001336038.1:n.19-86913T>C