Canonical Allele Identifier: CA472018907

Gene: TH

Linked Data

• MyVariant Identifiers: chr11:g.2191093C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2169863C>G , CM000673.2:g.2169863C>G	GRCh38
NC_000011.9:g.2191093C>G , CM000673.1:g.2191093C>G	GRCh37
NC_000011.8:g.2147669C>G	NCBI36
NG_008128.1:g.6943G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.99G>C MANE Select	ENSP00000325951.4:p.Arg33=
ENST00000324155.8:c.91-168G>C	ENSP00000325831.3:n.91-168G>C
ENST00000333684.9:c.99G>C	ENSP00000328814.6:p.Arg33=
ENST00000352909.7:c.99G>C	ENSP00000325951.3:p.Arg33=
ENST00000381168.7:c.103-168G>C	ENSP00000370560.3:n.103-168G>C
ENST00000381175.5:c.180G>C	ENSP00000370567.1:p.Arg60=
ENST00000381178.5:c.192G>C	ENSP00000370571.1:p.Arg64=
NM_000360.3:c.99G>C	NP_000351.2:p.Arg33=
NM_199292.2:c.192G>C	NP_954986.2:p.Arg64=
NM_199293.2:c.180G>C	NP_954987.2:p.Arg60=
XM_011520335.1:c.111G>C	XP_011518637.1:p.Arg37=
XM_011520335.2:c.111G>C	XP_011518637.1:p.Arg37=
NM_000360.4:c.99G>C MANE Select	NP_000351.2:p.Arg33=
NM_199292.3:c.192G>C	NP_954986.2:p.Arg64=
NM_199293.3:c.180G>C	NP_954987.2:p.Arg60=