Canonical Allele Identifier: CA1948012170
Gene: TH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2171813T= , CM000673.2:g.2171813T= GRCh38
NC_000011.9:g.2193043T= , CM000673.1:g.2193043T= GRCh37
NC_000011.8:g.2149619T= NCBI36
NG_008128.1:g.4993A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000352909.8:c.-27A= MANE Select ENSP00000325951.4:n.-27A=
ENST00000352909.7:c.-27A= ENSP00000325951.3:n.-27A=
XM_011520335.1:c.-27A= XP_011518637.1:n.-27A=
XM_011520335.2:c.-27A= XP_011518637.1:n.-27A=
NM_000360.4:c.-27A= MANE Select NP_000351.2:n.-27A=
NM_199292.3:c.-27A= NP_954986.2:n.-27A=
NM_199293.3:c.-27A= NP_954987.2:n.-27A=
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