Canonical Allele Identifier: CA1172975909
Gene: SLC35D1 HGNC NCBI

Linked Data

dbSNP Id: rs755977211
gnomAD v4: 1-67054049-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67054049T>G , CM000663.2:g.67054049T>G GRCh38
NC_000001.10:g.67519732T>G , CM000663.1:g.67519732T>G GRCh37
NC_000001.9:g.67292320T>G NCBI36
NG_012933.1:g.5349A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.-36A>C MANE Select ENSP00000235345.5:n.-36A>C
ENST00000235345.5:c.-36A>C ENSP00000235345.5:n.-36A>C
NM_015139.2:c.-36A>C NP_055954.1:n.-36A>C
XM_006710478.1:c.-36A>C XP_006710541.1:n.-36A>C
XM_011541070.1:c.-36A>C XP_011539372.1:n.-36A>C
XM_006710478.2:c.-36A>C XP_006710541.1:n.-36A>C
XM_011541070.2:c.-36A>C XP_011539372.1:n.-36A>C
XR_001737057.2:n.375A>C
XR_001737058.2:n.368A>C
NM_015139.3:c.-36A>C MANE Select NP_055954.1:n.-36A>C