Canonical Allele Identifier: CA1948012666
Gene: TH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2172191_2172198delinsAAAGCCCC , CM000673.2:g.2172191_2172198delinsAAAGCCCC GRCh38
NC_000011.9:g.2193421_2193428delinsAAAGCCCC , CM000673.1:g.2193421_2193428delinsAAAGCCCC GRCh37
NC_000011.8:g.2149997_2150004delinsAAAGCCCC NCBI36
NG_008128.1:g.4608_4615delinsGGGGCTTT

Transcript Alleles

HGVS Amino-acid Change
XM_011520335.2:c.-412_-405delinsGGGGCTTT XP_011518637.1:n.-412_-405delinsGGGGCTTT
Search 100 bp 5'
Search 100 bp 3'