Canonical Allele Identifier: CA591067150
Gene: DBH HGNC NCBI

Linked Data

dbSNP Id: rs1463678299
gnomAD v2: 9-136509337-CA-C
gnomAD v4: 9-133644215-CA-C
MyVariant Identifiers: chr9:g.136509338del (hg19) chr9:g.133644216del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644216del , CM000671.2:g.133644216del GRCh38
NC_000009.11:g.136509338del , CM000671.1:g.136509338del GRCh37
NC_000009.10:g.135499159del NCBI36
NG_008645.1:g.12854del

Transcript Alleles

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