Canonical Allele Identifier: CA2611984586
Gene: TH HGNC NCBI

Linked Data

gnomAD v4: 11-2171884-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2171884T>C , CM000673.2:g.2171884T>C GRCh38
NC_000011.9:g.2193114T>C , CM000673.1:g.2193114T>C GRCh37
NC_000011.8:g.2149690T>C NCBI36
NG_008128.1:g.4922A>G

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-98A>G XP_011518637.1:n.-98A>G
XM_011520335.2:c.-98A>G XP_011518637.1:n.-98A>G