Canonical Allele Identifier: CA137993132
Gene: SUPT3H HGNC NCBI

Linked Data

dbSNP Id: rs114899337
gnomAD v2: 6-44777711-C-T
gnomAD v3: 6-44809974-C-T
gnomAD v4: 6-44809974-C-T
MyVariant Identifiers: chr6:g.44777711C>T (hg19) chr6:g.44809974C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44809974C>T , CM000668.2:g.44809974C>T GRCh38
NC_000006.11:g.44777711C>T , CM000668.1:g.44777711C>T GRCh37
NC_000006.10:g.44885689C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000475057.5:c.*53-473G>A ENSP00000436411.1:n.*53-473G>A
XR_926319.1:n.1091-473G>A
XR_926854.1:n.341-19614C>T
XR_926855.1:n.172-19614C>T
NR_146632.1:n.1104-473G>A
NR_146633.1:n.1166-473G>A
NR_146634.1:n.1118-473G>A
NR_146635.1:n.1163-473G>A
XR_002956310.1:n.1432-473G>A
XR_926319.3:n.1091-473G>A
XR_926854.2:n.365-19614C>T
XR_926855.2:n.246-19614C>T
NR_146632.2:n.1174-473G>A
NR_146634.2:n.1160-473G>A
NR_146635.2:n.1307-473G>A
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