Canonical Allele Identifier: CA137993060
Gene: SUPT3H HGNC NCBI

Linked Data

dbSNP Id: rs542540047
gnomAD v2: 6-44777538-A-T
gnomAD v3: 6-44809801-A-T
gnomAD v4: 6-44809801-A-T
MyVariant Identifiers: chr6:g.44777538A>T (hg19) chr6:g.44809801A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.44809801A>T , CM000668.2:g.44809801A>T GRCh38
NC_000006.11:g.44777538A>T , CM000668.1:g.44777538A>T GRCh37
NC_000006.10:g.44885516A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000475057.5:c.*53-300T>A ENSP00000436411.1:n.*53-300T>A
XR_926319.1:n.1091-300T>A
XR_926854.1:n.341-19787A>T
XR_926855.1:n.172-19787A>T
NR_146632.1:n.1104-300T>A
NR_146633.1:n.1166-300T>A
NR_146634.1:n.1118-300T>A
NR_146635.1:n.1163-300T>A
XR_002956310.1:n.1432-300T>A
XR_926319.3:n.1091-300T>A
XR_926854.2:n.365-19787A>T
XR_926855.2:n.246-19787A>T
NR_146632.2:n.1174-300T>A
NR_146634.2:n.1160-300T>A
NR_146635.2:n.1307-300T>A
Search 100 bp 5'
Search 100 bp 3'