Canonical Allele Identifier: CA472018741

Gene: TH

Linked Data

• gnomAD v4: 11-2169670-G-T
• MyVariant Identifiers: chr11:g.2190900G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2169670G>T , CM000673.2:g.2169670G>T	GRCh38
NC_000011.9:g.2190900G>T , CM000673.1:g.2190900G>T	GRCh37
NC_000011.8:g.2147476G>T	NCBI36
NG_008128.1:g.7136C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000352909.8:c.292C>A MANE Select	ENSP00000325951.4:p.Arg98=
ENST00000324155.8:c.116C>A	ENSP00000325831.3:p.Pro39Gln
ENST00000333684.9:c.292C>A	ENSP00000328814.6:p.Arg98=
ENST00000352909.7:c.292C>A	ENSP00000325951.3:p.Arg98=
ENST00000381168.7:c.128C>A	ENSP00000370560.3:p.Pro43Gln
ENST00000381175.5:c.373C>A	ENSP00000370567.1:p.Arg125=
ENST00000381178.5:c.385C>A	ENSP00000370571.1:p.Arg129=
NM_000360.3:c.292C>A	NP_000351.2:p.Arg98=
NM_199292.2:c.385C>A	NP_954986.2:p.Arg129=
NM_199293.2:c.373C>A	NP_954987.2:p.Arg125=
XM_011520335.1:c.304C>A	XP_011518637.1:p.Arg102=
XM_011520335.2:c.304C>A	XP_011518637.1:p.Arg102=
NM_000360.4:c.292C>A MANE Select	NP_000351.2:p.Arg98=
NM_199292.3:c.385C>A	NP_954986.2:p.Arg129=
NM_199293.3:c.373C>A	NP_954987.2:p.Arg125=