Canonical Allele Identifier: CA2611985051
Gene: TH HGNC NCBI

Linked Data

gnomAD v4: 11-2172013-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172013T>C , CM000673.2:g.2172013T>C GRCh38
NC_000011.9:g.2193243T>C , CM000673.1:g.2193243T>C GRCh37
NC_000011.8:g.2149819T>C NCBI36
NG_008128.1:g.4793A>G

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-227A>G XP_011518637.1:n.-227A>G
XM_011520335.2:c.-227A>G XP_011518637.1:n.-227A>G