Canonical Allele Identifier: CA591067146
Gene: DBH HGNC NCBI

Linked Data

dbSNP Id: rs1427319517
gnomAD v2: 9-136509327-T-TTGCC
gnomAD v4: 9-133644205-T-TTGCC
MyVariant Identifiers: chr9:g.136509327_136509328insTGCC (hg19) chr9:g.133644205_133644206insTGCC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644206_133644209dup , CM000671.2:g.133644206_133644209dup GRCh38
NC_000009.11:g.136509328_136509331dup , CM000671.1:g.136509328_136509331dup GRCh37
NC_000009.10:g.135499149_135499152dup NCBI36
NG_008645.1:g.12844_12847dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.922-12_922-9dup MANE Select ENSP00000376776.2:n.922-12_922-9dup
ENST00000393056.6:c.922-12_922-9dup ENSP00000376776.2:n.922-12_922-9dup
NM_000787.3:c.922-12_922-9dup NP_000778.3:n.922-12_922-9dup
NM_000787.4:c.922-12_922-9dup MANE Select NP_000778.3:n.922-12_922-9dup
Search 100 bp 5'
Search 100 bp 3'