Canonical Allele Identifier: CA1948012301
Gene: TH HGNC NCBI

Linked Data

dbSNP Id: rs1846271865
gnomAD v4: 11-2171917-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2171917G>A , CM000673.2:g.2171917G>A GRCh38
NC_000011.9:g.2193147G>A , CM000673.1:g.2193147G>A GRCh37
NC_000011.8:g.2149723G>A NCBI36
NG_008128.1:g.4889C>T

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-131C>T XP_011518637.1:n.-131C>T
XM_011520335.2:c.-131C>T XP_011518637.1:n.-131C>T