Canonical Allele Identifier: CA379126111

Gene: TH

Linked Data

• MyVariant Identifiers: chr11:g.2187874G>C (hg19) ; chr11:g.2166644G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2166644G>C , CM000673.2:g.2166644G>C	GRCh38
NC_000011.9:g.2187874G>C , CM000673.1:g.2187874G>C	GRCh37
NC_000011.8:g.2144450G>C	NCBI36
NG_008128.1:g.10162C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.966C>G MANE Select	ENSP00000325951.4:p.His322Gln
ENST00000324155.8:c.*655C>G	ENSP00000325831.3:n.*655C>G
ENST00000333684.9:c.696-95C>G	ENSP00000328814.6:n.696-95C>G
ENST00000352909.7:c.966C>G	ENSP00000325951.3:p.His322Gln
ENST00000381168.7:c.*686C>G	ENSP00000370560.3:n.*686C>G
ENST00000381175.5:c.1047C>G	ENSP00000370567.1:p.His349Gln
ENST00000381178.5:c.1059C>G	ENSP00000370571.1:p.His353Gln
ENST00000412076.1:c.136-95C>G
ENST00000416223.5:c.260C>G
ENST00000461172.1:n.131C>G
ENST00000479437.5:n.515C>G
NM_000360.3:c.966C>G	NP_000351.2:p.His322Gln
NM_199292.2:c.1059C>G	NP_954986.2:p.His353Gln
NM_199293.2:c.1047C>G	NP_954987.2:p.His349Gln
XM_011520335.1:c.978C>G	XP_011518637.1:p.His326Gln
XM_011520335.2:c.978C>G	XP_011518637.1:p.His326Gln
NM_000360.4:c.966C>G MANE Select	NP_000351.2:p.His322Gln
NM_199292.3:c.1059C>G	NP_954986.2:p.His353Gln
NM_199293.3:c.1047C>G	NP_954987.2:p.His349Gln