Canonical Allele Identifier: CA825049164

Gene: SUPT3H

Linked Data

• dbSNP Id: rs1310201882
• MyVariant Identifiers: chr6:g.44777836_44777837insT (hg19) ; chr6:g.44810099_44810100insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.44810099_44810100insT , CM000668.2:g.44810099_44810100insT	GRCh38
NC_000006.11:g.44777836_44777837insT , CM000668.1:g.44777836_44777837insT	GRCh37
NC_000006.10:g.44885814_44885815insT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475057.5:c.*53-599_*53-598insA	ENSP00000436411.1:n.*53-599_*53-598insA
XR_926319.1:n.1091-599_1091-598insA
XR_926854.1:n.341-19489_341-19488insT
XR_926855.1:n.172-19489_172-19488insT
NR_146632.1:n.1104-599_1104-598insA
NR_146633.1:n.1166-599_1166-598insA
NR_146634.1:n.1118-599_1118-598insA
NR_146635.1:n.1163-599_1163-598insA
XR_002956310.1:n.1432-599_1432-598insA
XR_926319.3:n.1091-599_1091-598insA
XR_926854.2:n.365-19489_365-19488insT
XR_926855.2:n.246-19489_246-19488insT
NR_146632.2:n.1174-599_1174-598insA
NR_146634.2:n.1160-599_1160-598insA
NR_146635.2:n.1307-599_1307-598insA