Canonical Allele Identifier: CA1948012522
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172065G= , CM000673.2:g.2172065G= GRCh38
NC_000011.9:g.2193295G= , CM000673.1:g.2193295G= GRCh37
NC_000011.8:g.2149871G= NCBI36
NG_008128.1:g.4741C=

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-279C= XP_011518637.1:n.-279C=
XM_011520335.2:c.-279C= XP_011518637.1:n.-279C=