Canonical Allele Identifier: CA1002733724
Gene: SLC35D1 HGNC NCBI

Linked Data

dbSNP Id: rs1645347199
gnomAD v3: 1-67054113-G-C
gnomAD v4: 1-67054113-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67054113G>C , CM000663.2:g.67054113G>C GRCh38
NC_000001.10:g.67519796G>C , CM000663.1:g.67519796G>C GRCh37
NC_000001.9:g.67292384G>C NCBI36
NG_012933.1:g.5285C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.-100C>G MANE Select ENSP00000235345.5:n.-100C>G
NM_015139.2:c.-100C>G NP_055954.1:n.-100C>G
XM_006710478.1:c.-100C>G XP_006710541.1:n.-100C>G
XM_011541070.1:c.-100C>G XP_011539372.1:n.-100C>G
XM_006710478.2:c.-100C>G XP_006710541.1:n.-100C>G
XM_011541070.2:c.-100C>G XP_011539372.1:n.-100C>G
XR_001737057.2:n.311C>G
XR_001737058.2:n.304C>G
NM_015139.3:c.-100C>G MANE Select NP_055954.1:n.-100C>G