Canonical Allele Identifier: CA2611984383
Gene: TH HGNC NCBI

Linked Data

gnomAD v4: 11-2171841-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2171841T>G , CM000673.2:g.2171841T>G GRCh38
NC_000011.9:g.2193071T>G , CM000673.1:g.2193071T>G GRCh37
NC_000011.8:g.2149647T>G NCBI36
NG_008128.1:g.4965A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000352909.7:c.-55A>C ENSP00000325951.3:n.-55A>C
XM_011520335.1:c.-55A>C XP_011518637.1:n.-55A>C
XM_011520335.2:c.-55A>C XP_011518637.1:n.-55A>C