Canonical Allele Identifier: CA137993104
Gene: SUPT3H HGNC NCBI

Linked Data

dbSNP Id: rs767622267
gnomAD v2: 6-44777680-G-T
gnomAD v3: 6-44809943-G-T
gnomAD v4: 6-44809943-G-T
MyVariant Identifiers: chr6:g.44777680G>T (hg19) chr6:g.44809943G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44809943G>T , CM000668.2:g.44809943G>T GRCh38
NC_000006.11:g.44777680G>T , CM000668.1:g.44777680G>T GRCh37
NC_000006.10:g.44885658G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000475057.5:c.*53-442C>A ENSP00000436411.1:n.*53-442C>A
XR_926319.1:n.1091-442C>A
XR_926854.1:n.341-19645G>T
XR_926855.1:n.172-19645G>T
NR_146632.1:n.1104-442C>A
NR_146633.1:n.1166-442C>A
NR_146634.1:n.1118-442C>A
NR_146635.1:n.1163-442C>A
XR_002956310.1:n.1432-442C>A
XR_926319.3:n.1091-442C>A
XR_926854.2:n.365-19645G>T
XR_926855.2:n.246-19645G>T
NR_146632.2:n.1174-442C>A
NR_146634.2:n.1160-442C>A
NR_146635.2:n.1307-442C>A
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