Canonical Allele Identifier: CA566955578

Gene: SUPT3H

Linked Data

• dbSNP Id: rs1421959032
• gnomAD v2: 6-44777777-A-C
• gnomAD v3: 6-44810040-A-C
• gnomAD v4: 6-44810040-A-C
• MyVariant Identifiers: chr6:g.44777777A>C (hg19) ; chr6:g.44810040A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.44810040A>C , CM000668.2:g.44810040A>C	GRCh38
NC_000006.11:g.44777777A>C , CM000668.1:g.44777777A>C	GRCh37
NC_000006.10:g.44885755A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475057.5:c.*53-539T>G	ENSP00000436411.1:n.*53-539T>G
XR_926319.1:n.1091-539T>G
XR_926854.1:n.341-19548A>C
XR_926855.1:n.172-19548A>C
NR_146632.1:n.1104-539T>G
NR_146633.1:n.1166-539T>G
NR_146634.1:n.1118-539T>G
NR_146635.1:n.1163-539T>G
XR_002956310.1:n.1432-539T>G
XR_926319.3:n.1091-539T>G
XR_926854.2:n.365-19548A>C
XR_926855.2:n.246-19548A>C
NR_146632.2:n.1174-539T>G
NR_146634.2:n.1160-539T>G
NR_146635.2:n.1307-539T>G