Canonical Allele Identifier: CA2790190910
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2171993C>T , CM000673.2:g.2171993C>T GRCh38
NC_000011.9:g.2193223C>T , CM000673.1:g.2193223C>T GRCh37
NC_000011.8:g.2149799C>T NCBI36
NG_008128.1:g.4813G>A

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-207G>A XP_011518637.1:n.-207G>A
XM_011520335.2:c.-207G>A XP_011518637.1:n.-207G>A