Canonical Allele Identifier: CA1002733692
Gene: SLC35D1 HGNC NCBI

Linked Data

dbSNP Id: rs1645346601
gnomAD v3: 1-67054076-C-T
gnomAD v4: 1-67054076-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67054076C>T , CM000663.2:g.67054076C>T GRCh38
NC_000001.10:g.67519759C>T , CM000663.1:g.67519759C>T GRCh37
NC_000001.9:g.67292347C>T NCBI36
NG_012933.1:g.5322G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.-63G>A MANE Select ENSP00000235345.5:n.-63G>A
ENST00000235345.5:c.-63G>A ENSP00000235345.5:n.-63G>A
NM_015139.2:c.-63G>A NP_055954.1:n.-63G>A
XM_006710478.1:c.-63G>A XP_006710541.1:n.-63G>A
XM_011541070.1:c.-63G>A XP_011539372.1:n.-63G>A
XM_006710478.2:c.-63G>A XP_006710541.1:n.-63G>A
XM_011541070.2:c.-63G>A XP_011539372.1:n.-63G>A
XR_001737057.2:n.348G>A
XR_001737058.2:n.341G>A
NM_015139.3:c.-63G>A MANE Select NP_055954.1:n.-63G>A
Search 100 bp 5'
Search 100 bp 3'