Canonical Allele Identifier: CA1882777217
Gene: DBH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644297A= , CM000671.2:g.133644297A= GRCh38
NC_000009.11:g.136509419A= , CM000671.1:g.136509419A= GRCh37
NC_000009.10:g.135499240A= NCBI36
NG_008645.1:g.12935A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000393056.8:c.1001A= MANE Select ENSP00000376776.2:p.Tyr334=
ENST00000393056.6:c.1001A= ENSP00000376776.2:p.Tyr334=
NM_000787.3:c.1001A= NP_000778.3:p.Tyr334=
NM_000787.4:c.1001A= MANE Select NP_000778.3:p.Tyr334=
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