Canonical Allele Identifier: CA379126313

Gene: TH

Linked Data

• gnomAD v4: 11-2166736-C-G
• MyVariant Identifiers: chr11:g.2187966C>G (hg19) ; chr11:g.2166736C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2166736C>G , CM000673.2:g.2166736C>G	GRCh38
NC_000011.9:g.2187966C>G , CM000673.1:g.2187966C>G	GRCh37
NC_000011.8:g.2144542C>G	NCBI36
NG_008128.1:g.10070G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.874G>C MANE Select	ENSP00000325951.4:p.Gly292Arg
ENST00000324155.8:c.*563G>C	ENSP00000325831.3:n.*563G>C
ENST00000333684.9:c.696-187G>C	ENSP00000328814.6:n.696-187G>C
ENST00000352909.7:c.874G>C	ENSP00000325951.3:p.Gly292Arg
ENST00000381168.7:c.*594G>C	ENSP00000370560.3:n.*594G>C
ENST00000381175.5:c.955G>C	ENSP00000370567.1:p.Gly319Arg
ENST00000381178.5:c.967G>C	ENSP00000370571.1:p.Gly323Arg
ENST00000412076.1:c.136-187G>C
ENST00000416223.5:c.168G>C
ENST00000461172.1:n.39G>C
ENST00000479437.5:n.423G>C
NM_000360.3:c.874G>C	NP_000351.2:p.Gly292Arg
NM_199292.2:c.967G>C	NP_954986.2:p.Gly323Arg
NM_199293.2:c.955G>C	NP_954987.2:p.Gly319Arg
XM_011520335.1:c.886G>C	XP_011518637.1:p.Gly296Arg
XM_011520335.2:c.886G>C	XP_011518637.1:p.Gly296Arg
NM_000360.4:c.874G>C MANE Select	NP_000351.2:p.Gly292Arg
NM_199292.3:c.967G>C	NP_954986.2:p.Gly323Arg
NM_199293.3:c.955G>C	NP_954987.2:p.Gly319Arg