Canonical Allele Identifier: CA674607029

Gene: TH

Linked Data

• ClinVar Variation Id: 1396605
• ClinVar RCV Id: RCV001903066
• dbSNP Id: rs528887823
• gnomAD v4: 11-2166884-C-T
• MyVariant Identifiers: chr11:g.2188114C>T (hg19) ; chr11:g.2166884C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2166884C>T , CM000673.2:g.2166884C>T	GRCh38
NC_000011.9:g.2188114C>T , CM000673.1:g.2188114C>T	GRCh37
NC_000011.8:g.2144690C>T	NCBI36
NG_008128.1:g.9922G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.841+3G>A MANE Select	ENSP00000325951.4:n.841+3G>A
ENST00000324155.8:c.*530+3G>A	ENSP00000325831.3:n.*530+3G>A
ENST00000333684.9:c.696-335G>A	ENSP00000328814.6:n.696-335G>A
ENST00000352909.7:c.841+3G>A	ENSP00000325951.3:n.841+3G>A
ENST00000381168.7:c.*561+3G>A	ENSP00000370560.3:n.*561+3G>A
ENST00000381175.5:c.922+3G>A	ENSP00000370567.1:n.922+3G>A
ENST00000381178.5:c.934+3G>A	ENSP00000370571.1:n.934+3G>A
ENST00000412076.1:c.136-335G>A
ENST00000416223.5:c.136-116G>A
ENST00000479437.5:n.390+3G>A
NM_000360.3:c.841+3G>A	NP_000351.2:n.841+3G>A
NM_199292.2:c.934+3G>A	NP_954986.2:n.934+3G>A
NM_199293.2:c.922+3G>A	NP_954987.2:n.922+3G>A
XM_011520335.1:c.853+3G>A	XP_011518637.1:n.853+3G>A
XM_011520335.2:c.853+3G>A	XP_011518637.1:n.853+3G>A
NM_000360.4:c.841+3G>A MANE Select	NP_000351.2:n.841+3G>A
NM_199292.3:c.934+3G>A	NP_954986.2:n.934+3G>A
NM_199293.3:c.922+3G>A	NP_954987.2:n.922+3G>A