Canonical Allele Identifier: CA1948012653
Gene: TH HGNC NCBI

Linked Data

dbSNP Id: rs1846278329
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172180G>A , CM000673.2:g.2172180G>A GRCh38
NC_000011.9:g.2193410G>A , CM000673.1:g.2193410G>A GRCh37
NC_000011.8:g.2149986G>A NCBI36
NG_008128.1:g.4626C>T

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.2:c.-394C>T XP_011518637.1:n.-394C>T
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Search 100 bp 3'