Canonical Allele Identifier: CA899231
Gene: SLC35D1 HGNC NCBI

Linked Data

dbSNP Id: rs371509595
ExAC: 1:67519745 G / T
gnomAD v2: 1-67519745-G-T
gnomAD v3: 1-67054062-G-T
gnomAD v4: 1-67054062-G-T
MyVariant Identifiers: chr1:g.67519745G>T (hg19) chr1:g.67054062G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.67054062G>T , CM000663.2:g.67054062G>T GRCh38
NC_000001.10:g.67519745G>T , CM000663.1:g.67519745G>T GRCh37
NC_000001.9:g.67292333G>T NCBI36
NG_012933.1:g.5336C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000235345.6:c.-49C>A MANE Select ENSP00000235345.5:n.-49C>A
ENST00000235345.5:c.-49C>A ENSP00000235345.5:n.-49C>A
NM_015139.2:c.-49C>A NP_055954.1:n.-49C>A
XM_006710478.1:c.-49C>A XP_006710541.1:n.-49C>A
XM_011541070.1:c.-49C>A XP_011539372.1:n.-49C>A
XM_006710478.2:c.-49C>A XP_006710541.1:n.-49C>A
XM_011541070.2:c.-49C>A XP_011539372.1:n.-49C>A
XR_001737057.2:n.362C>A
XR_001737058.2:n.355C>A
NM_015139.3:c.-49C>A MANE Select NP_055954.1:n.-49C>A
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