Canonical Allele Identifier: CA467613738
Gene: DBH HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136509342A>T (hg19)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.924A>T MANE Select ENSP00000376776.2:p.Ala308=
ENST00000393056.6:c.924A>T ENSP00000376776.2:p.Ala308=
NM_000787.3:c.924A>T NP_000778.3:p.Ala308=
NM_000787.4:c.924A>T MANE Select NP_000778.3:p.Ala308=
Search 100 bp 5'
Search 100 bp 3'