Canonical Allele Identifier: CA1948012314
Gene: TH HGNC NCBI

Linked Data

dbSNP Id: rs1213067228

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2171936del , CM000673.2:g.2171936del GRCh38
NC_000011.9:g.2193166del , CM000673.1:g.2193166del GRCh37
NC_000011.8:g.2149742del NCBI36
NG_008128.1:g.4874del

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.1:c.-146del XP_011518637.1:n.-146del
XM_011520335.2:c.-146del XP_011518637.1:n.-146del