Canonical Allele Identifier: CA137993100

Gene: SUPT3H

Linked Data

• dbSNP Id: rs532551823
• gnomAD v2: 6-44777657-G-T
• gnomAD v3: 6-44809920-G-T
• gnomAD v4: 6-44809920-G-T
• MyVariant Identifiers: chr6:g.44777657G>T (hg19) ; chr6:g.44809920G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.44809920G>T , CM000668.2:g.44809920G>T	GRCh38
NC_000006.11:g.44777657G>T , CM000668.1:g.44777657G>T	GRCh37
NC_000006.10:g.44885635G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475057.5:c.*53-419C>A	ENSP00000436411.1:n.*53-419C>A
XR_926319.1:n.1091-419C>A
XR_926854.1:n.341-19668G>T
XR_926855.1:n.172-19668G>T
NR_146632.1:n.1104-419C>A
NR_146633.1:n.1166-419C>A
NR_146634.1:n.1118-419C>A
NR_146635.1:n.1163-419C>A
XR_002956310.1:n.1432-419C>A
XR_926319.3:n.1091-419C>A
XR_926854.2:n.365-19668G>T
XR_926855.2:n.246-19668G>T
NR_146632.2:n.1174-419C>A
NR_146634.2:n.1160-419C>A
NR_146635.2:n.1307-419C>A