Canonical Allele Identifier: CA5818741

Gene: TH

Linked Data

• ClinVar Variation Id: 1120612
• ClinVar RCV Id: RCV001450594
• dbSNP Id: rs75348531
• ExAC: 11:2190910 C / G
• gnomAD v2: 11-2190910-C-G
• gnomAD v3: 11-2169680-C-G
• gnomAD v4: 11-2169680-C-G
• MyVariant Identifiers: chr11:g.2190910C>G (hg19) ; chr11:g.2169680C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2169680C>G , CM000673.2:g.2169680C>G	GRCh38
NC_000011.9:g.2190910C>G , CM000673.1:g.2190910C>G	GRCh37
NC_000011.8:g.2147486C>G	NCBI36
NG_008128.1:g.7126G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000352909.8:c.282G>C MANE Select	ENSP00000325951.4:p.Ser94=
ENST00000324155.8:c.106G>C	ENSP00000325831.3:p.Gly36Arg
ENST00000333684.9:c.282G>C	ENSP00000328814.6:p.Ser94=
ENST00000352909.7:c.282G>C	ENSP00000325951.3:p.Ser94=
ENST00000381168.7:c.118G>C	ENSP00000370560.3:p.Gly40Arg
ENST00000381175.5:c.363G>C	ENSP00000370567.1:p.Ser121=
ENST00000381178.5:c.375G>C	ENSP00000370571.1:p.Ser125=
NM_000360.3:c.282G>C	NP_000351.2:p.Ser94=
NM_199292.2:c.375G>C	NP_954986.2:p.Ser125=
NM_199293.2:c.363G>C	NP_954987.2:p.Ser121=
XM_011520335.1:c.294G>C	XP_011518637.1:p.Ser98=
XM_011520335.2:c.294G>C	XP_011518637.1:p.Ser98=
NM_000360.4:c.282G>C MANE Select	NP_000351.2:p.Ser94=
NM_199292.3:c.375G>C	NP_954986.2:p.Ser125=
NM_199293.3:c.363G>C	NP_954987.2:p.Ser121=