Canonical Allele Identifier: CA137993107
Gene: SUPT3H HGNC NCBI

Linked Data

dbSNP Id: rs964440918
gnomAD v2: 6-44777681-A-G
gnomAD v3: 6-44809944-A-G
gnomAD v4: 6-44809944-A-G
MyVariant Identifiers: chr6:g.44777681A>G (hg19) chr6:g.44809944A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44809944A>G , CM000668.2:g.44809944A>G GRCh38
NC_000006.11:g.44777681A>G , CM000668.1:g.44777681A>G GRCh37
NC_000006.10:g.44885659A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000475057.5:c.*53-443T>C ENSP00000436411.1:n.*53-443T>C
XR_926319.1:n.1091-443T>C
XR_926854.1:n.341-19644A>G
XR_926855.1:n.172-19644A>G
NR_146632.1:n.1104-443T>C
NR_146633.1:n.1166-443T>C
NR_146634.1:n.1118-443T>C
NR_146635.1:n.1163-443T>C
XR_002956310.1:n.1432-443T>C
XR_926319.3:n.1091-443T>C
XR_926854.2:n.365-19644A>G
XR_926855.2:n.246-19644A>G
NR_146632.2:n.1174-443T>C
NR_146634.2:n.1160-443T>C
NR_146635.2:n.1307-443T>C
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