Canonical Allele Identifier: CA1948012515
Gene: TH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172063_2172064delinsCG , CM000673.2:g.2172063_2172064delinsCG GRCh38
NC_000011.9:g.2193293_2193294delinsCG , CM000673.1:g.2193293_2193294delinsCG GRCh37
NC_000011.8:g.2149869_2149870delinsCG NCBI36
NG_008128.1:g.4742_4743delinsCG

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-278_-277delinsCG XP_011518637.1:n.-278_-277delinsCG
XM_011520335.2:c.-278_-277delinsCG XP_011518637.1:n.-278_-277delinsCG