Canonical Allele Identifier: CA899200
Gene: SLC35D1 HGNC NCBI

Linked Data

dbSNP Id: rs377374951
ExAC: 1:67519679 T / C
gnomAD v2: 1-67519679-T-C
gnomAD v3: 1-67053996-T-C
gnomAD v4: 1-67053996-T-C
MyVariant Identifiers: chr1:g.67519679T>C (hg19) chr1:g.67053996T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67053996T>C , CM000663.2:g.67053996T>C GRCh38
NC_000001.10:g.67519679T>C , CM000663.1:g.67519679T>C GRCh37
NC_000001.9:g.67292267T>C NCBI36
NG_012933.1:g.5402A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.18A>G MANE Select ENSP00000235345.5:p.Arg6=
ENST00000235345.5:c.18A>G ENSP00000235345.5:p.Arg6=
NM_015139.2:c.18A>G NP_055954.1:p.Arg6=
XM_006710478.1:c.18A>G XP_006710541.1:p.Arg6=
XM_011541070.1:c.18A>G XP_011539372.1:p.Arg6=
XM_006710478.2:c.18A>G XP_006710541.1:p.Arg6=
XM_011541070.2:c.18A>G XP_011539372.1:p.Arg6=
XR_001737057.2:n.428A>G
XR_001737058.2:n.421A>G
NM_015139.3:c.18A>G MANE Select NP_055954.1:p.Arg6=
Search 100 bp 5'
Search 100 bp 3'