Canonical Allele Identifier: CA1172976008
Gene: SLC35D1 HGNC NCBI

Linked Data

dbSNP Id: rs1645347140
gnomAD v4: 1-67054110-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67054110C>T , CM000663.2:g.67054110C>T GRCh38
NC_000001.10:g.67519793C>T , CM000663.1:g.67519793C>T GRCh37
NC_000001.9:g.67292381C>T NCBI36
NG_012933.1:g.5288G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.-97G>A MANE Select ENSP00000235345.5:n.-97G>A
NM_015139.2:c.-97G>A NP_055954.1:n.-97G>A
XM_006710478.1:c.-97G>A XP_006710541.1:n.-97G>A
XM_011541070.1:c.-97G>A XP_011539372.1:n.-97G>A
XM_006710478.2:c.-97G>A XP_006710541.1:n.-97G>A
XM_011541070.2:c.-97G>A XP_011539372.1:n.-97G>A
XR_001737057.2:n.314G>A
XR_001737058.2:n.307G>A
NM_015139.3:c.-97G>A MANE Select NP_055954.1:n.-97G>A
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