Canonical Allele Identifier: CA523607682
Gene: SLC35D1 HGNC NCBI

Linked Data

dbSNP Id: rs1377255326
gnomAD v2: 1-67519765-G-A
gnomAD v3: 1-67054082-G-A
gnomAD v4: 1-67054082-G-A
MyVariant Identifiers: chr1:g.67519765G>A (hg19) chr1:g.67054082G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67054082G>A , CM000663.2:g.67054082G>A GRCh38
NC_000001.10:g.67519765G>A , CM000663.1:g.67519765G>A GRCh37
NC_000001.9:g.67292353G>A NCBI36
NG_012933.1:g.5316C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.-69C>T MANE Select ENSP00000235345.5:n.-69C>T
ENST00000235345.5:c.-69C>T ENSP00000235345.5:n.-69C>T
NM_015139.2:c.-69C>T NP_055954.1:n.-69C>T
XM_006710478.1:c.-69C>T XP_006710541.1:n.-69C>T
XM_011541070.1:c.-69C>T XP_011539372.1:n.-69C>T
XM_006710478.2:c.-69C>T XP_006710541.1:n.-69C>T
XM_011541070.2:c.-69C>T XP_011539372.1:n.-69C>T
XR_001737057.2:n.342C>T
XR_001737058.2:n.335C>T
NM_015139.3:c.-69C>T MANE Select NP_055954.1:n.-69C>T
Search 100 bp 5'
Search 100 bp 3'