Canonical Allele Identifier: CA5818760
Gene: TH HGNC NCBI

Linked Data

dbSNP Id: rs374853290
gnomAD v2: 11-2190987-C-G
gnomAD v3: 11-2169757-C-G
gnomAD v4: 11-2169757-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2169757C>G , CM000673.2:g.2169757C>G GRCh38
NC_000011.9:g.2190987C>G , CM000673.1:g.2190987C>G GRCh37
NC_000011.8:g.2147563C>G NCBI36
NG_008128.1:g.7049G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000352909.8:c.205G>C MANE Select ENSP00000325951.4:p.Glu69Gln
ENST00000324155.8:c.91-62G>C ENSP00000325831.3:n.91-62G>C
ENST00000333684.9:c.205G>C ENSP00000328814.6:p.Glu69Gln
ENST00000352909.7:c.205G>C ENSP00000325951.3:p.Glu69Gln
ENST00000381168.7:c.103-62G>C ENSP00000370560.3:n.103-62G>C
ENST00000381175.5:c.286G>C ENSP00000370567.1:p.Glu96Gln
ENST00000381178.5:c.298G>C ENSP00000370571.1:p.Glu100Gln
NM_000360.3:c.205G>C NP_000351.2:p.Glu69Gln
NM_199292.2:c.298G>C NP_954986.2:p.Glu100Gln
NM_199293.2:c.286G>C NP_954987.2:p.Glu96Gln
XM_011520335.1:c.217G>C XP_011518637.1:p.Glu73Gln
XM_011520335.2:c.217G>C XP_011518637.1:p.Glu73Gln
NM_000360.4:c.205G>C MANE Select NP_000351.2:p.Glu69Gln
NM_199292.3:c.298G>C NP_954986.2:p.Glu100Gln
NM_199293.3:c.286G>C NP_954987.2:p.Glu96Gln