Canonical Allele Identifier: CA1625150169
Gene: SUPT3H HGNC NCBI

Linked Data

dbSNP Id: rs1766392187
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44809865A>G , CM000668.2:g.44809865A>G GRCh38
NC_000006.11:g.44777602A>G , CM000668.1:g.44777602A>G GRCh37
NC_000006.10:g.44885580A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000475057.5:c.*53-364T>C ENSP00000436411.1:n.*53-364T>C
XR_926319.1:n.1091-364T>C
XR_926854.1:n.341-19723A>G
XR_926855.1:n.172-19723A>G
NR_146632.1:n.1104-364T>C
NR_146633.1:n.1166-364T>C
NR_146634.1:n.1118-364T>C
NR_146635.1:n.1163-364T>C
XR_002956310.1:n.1432-364T>C
XR_926319.3:n.1091-364T>C
XR_926854.2:n.365-19723A>G
XR_926855.2:n.246-19723A>G
NR_146632.2:n.1174-364T>C
NR_146634.2:n.1160-364T>C
NR_146635.2:n.1307-364T>C
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