Canonical Allele Identifier: CA5818795

Gene: TH

Linked Data

• ClinVar Variation Id: 701386
• ClinVar RCV Id: RCV000869905
• dbSNP Id: rs202167640
• ExAC: 11:2191096 C / T
• gnomAD v2: 11-2191096-C-T
• gnomAD v3: 11-2169866-C-T
• gnomAD v4: 11-2169866-C-T
• MyVariant Identifiers: chr11:g.2191096C>T (hg19) ; chr11:g.2169866C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2169866C>T , CM000673.2:g.2169866C>T	GRCh38
NC_000011.9:g.2191096C>T , CM000673.1:g.2191096C>T	GRCh37
NC_000011.8:g.2147672C>T	NCBI36
NG_008128.1:g.6940G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.96G>A MANE Select	ENSP00000325951.4:p.Pro32=
ENST00000324155.8:c.91-171G>A	ENSP00000325831.3:n.91-171G>A
ENST00000333684.9:c.96G>A	ENSP00000328814.6:p.Pro32=
ENST00000352909.7:c.96G>A	ENSP00000325951.3:p.Pro32=
ENST00000381168.7:c.103-171G>A	ENSP00000370560.3:n.103-171G>A
ENST00000381175.5:c.177G>A	ENSP00000370567.1:p.Pro59=
ENST00000381178.5:c.189G>A	ENSP00000370571.1:p.Pro63=
NM_000360.3:c.96G>A	NP_000351.2:p.Pro32=
NM_199292.2:c.189G>A	NP_954986.2:p.Pro63=
NM_199293.2:c.177G>A	NP_954987.2:p.Pro59=
XM_011520335.1:c.108G>A	XP_011518637.1:p.Pro36=
XM_011520335.2:c.108G>A	XP_011518637.1:p.Pro36=
NM_000360.4:c.96G>A MANE Select	NP_000351.2:p.Pro32=
NM_199292.3:c.189G>A	NP_954986.2:p.Pro63=
NM_199293.3:c.177G>A	NP_954987.2:p.Pro59=