Canonical Allele Identifier: CA200963809
Gene: DBH HGNC NCBI

Linked Data

dbSNP Id: rs1053895722
gnomAD v3: 9-133644220-A-C
gnomAD v4: 9-133644220-A-C
MyVariant Identifiers: chr9:g.136509342A>C (hg19) chr9:g.133644220A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644220A>C , CM000671.2:g.133644220A>C GRCh38
NC_000009.11:g.136509342A>C , CM000671.1:g.136509342A>C GRCh37
NC_000009.10:g.135499163A>C NCBI36
NG_008645.1:g.12858A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.924A>C MANE Select ENSP00000376776.2:p.Ala308=
ENST00000393056.6:c.924A>C ENSP00000376776.2:p.Ala308=
NM_000787.3:c.924A>C NP_000778.3:p.Ala308=
NM_000787.4:c.924A>C MANE Select NP_000778.3:p.Ala308=
Search 100 bp 5'
Search 100 bp 3'