Canonical Allele Identifier: CA1948012502
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172056T= , CM000673.2:g.2172056T= GRCh38
NC_000011.9:g.2193286T= , CM000673.1:g.2193286T= GRCh37
NC_000011.8:g.2149862T= NCBI36
NG_008128.1:g.4750A=

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-270A= XP_011518637.1:n.-270A=
XM_011520335.2:c.-270A= XP_011518637.1:n.-270A=