Canonical Allele Identifier: CA2692393540
Gene: DBH HGNC NCBI

Linked Data

gnomAD v4: 9-133644397-TCGTCTGCCCAGCATGGTGCCCCCGCTGTACAGCTCCTCTTGGCACGAGGCCCTTG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644406_133644460del , CM000671.2:g.133644406_133644460del GRCh38
NC_000009.11:g.136509528_136509582del , CM000671.1:g.136509528_136509582del GRCh37
NC_000009.10:g.135499349_135499403del NCBI36
NG_008645.1:g.13044_13098del

Transcript Alleles

HGVS Amino-acid change
ENST00000393056.8:c.1024+86_1024+140del MANE Select ENSP00000376776.2:n.1024+86_1024+140del
ENST00000393056.6:c.1024+86_1024+140del ENSP00000376776.2:n.1024+86_1024+140del
NM_000787.3:c.1024+86_1024+140del NP_000778.3:n.1024+86_1024+140del
NM_000787.4:c.1024+86_1024+140del MANE Select NP_000778.3:n.1024+86_1024+140del
Search 100 bp 5'
Search 100 bp 3'