Canonical Allele Identifier: CA200964102
Gene: DBH HGNC NCBI

Linked Data

dbSNP Id: rs993475126
gnomAD v2: 9-136509542-C-T
gnomAD v3: 9-133644420-C-T
gnomAD v4: 9-133644420-C-T
MyVariant Identifiers: chr9:g.136509542C>T (hg19) chr9:g.133644420C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644420C>T , CM000671.2:g.133644420C>T GRCh38
NC_000009.11:g.136509542C>T , CM000671.1:g.136509542C>T GRCh37
NC_000009.10:g.135499363C>T NCBI36
NG_008645.1:g.13058C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000393056.8:c.1024+100C>T MANE Select ENSP00000376776.2:n.1024+100C>T
ENST00000393056.6:c.1024+100C>T ENSP00000376776.2:n.1024+100C>T
NM_000787.3:c.1024+100C>T NP_000778.3:n.1024+100C>T
NM_000787.4:c.1024+100C>T MANE Select NP_000778.3:n.1024+100C>T
Search 100 bp 5'
Search 100 bp 3'