Canonical Allele Identifier: CA1948012480
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172044A= , CM000673.2:g.2172044A= GRCh38
NC_000011.9:g.2193274A= , CM000673.1:g.2193274A= GRCh37
NC_000011.8:g.2149850A= NCBI36
NG_008128.1:g.4762T=

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-258T= XP_011518637.1:n.-258T=
XM_011520335.2:c.-258T= XP_011518637.1:n.-258T=