Canonical Allele Identifier: CA1948012331
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2171942_2171943delinsGA , CM000673.2:g.2171942_2171943delinsGA GRCh38
NC_000011.9:g.2193172_2193173delinsGA , CM000673.1:g.2193172_2193173delinsGA GRCh37
NC_000011.8:g.2149748_2149749delinsGA NCBI36
NG_008128.1:g.4863_4864delinsTC

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-157_-156delinsTC XP_011518637.1:n.-157_-156delinsTC
XM_011520335.2:c.-157_-156delinsTC XP_011518637.1:n.-157_-156delinsTC