Canonical Allele Identifier: CA2611985061
Gene: TH HGNC NCBI

Linked Data

gnomAD v4: 11-2172017-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172017T>A , CM000673.2:g.2172017T>A GRCh38
NC_000011.9:g.2193247T>A , CM000673.1:g.2193247T>A GRCh37
NC_000011.8:g.2149823T>A NCBI36
NG_008128.1:g.4789A>T

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-231A>T XP_011518637.1:n.-231A>T
XM_011520335.2:c.-231A>T XP_011518637.1:n.-231A>T