Canonical Allele Identifier: CA899221
Gene: SLC35D1 HGNC NCBI

Linked Data

dbSNP Id: rs554051043
ExAC: 1:67519726 G / C
gnomAD v2: 1-67519726-G-C
gnomAD v3: 1-67054043-G-C
gnomAD v4: 1-67054043-G-C
MyVariant Identifiers: chr1:g.67519726G>C (hg19) chr1:g.67054043G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67054043G>C , CM000663.2:g.67054043G>C GRCh38
NC_000001.10:g.67519726G>C , CM000663.1:g.67519726G>C GRCh37
NC_000001.9:g.67292314G>C NCBI36
NG_012933.1:g.5355C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.-30C>G MANE Select ENSP00000235345.5:n.-30C>G
ENST00000235345.5:c.-30C>G ENSP00000235345.5:n.-30C>G
NM_015139.2:c.-30C>G NP_055954.1:n.-30C>G
XM_006710478.1:c.-30C>G XP_006710541.1:n.-30C>G
XM_011541070.1:c.-30C>G XP_011539372.1:n.-30C>G
XM_006710478.2:c.-30C>G XP_006710541.1:n.-30C>G
XM_011541070.2:c.-30C>G XP_011539372.1:n.-30C>G
XR_001737057.2:n.381C>G
XR_001737058.2:n.374C>G
NM_015139.3:c.-30C>G MANE Select NP_055954.1:n.-30C>G
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