Canonical Allele Identifier: CA1882770218
Gene: DBH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133638725A= , CM000671.2:g.133638725A= GRCh38
NC_000009.11:g.136503847A= , CM000671.1:g.136503847A= GRCh37
NC_000009.10:g.135493668A= NCBI36
NG_008645.1:g.7363A=

Transcript Alleles

HGVS Amino-acid change
ENST00000263611.3:c.333+2015A= ENSP00000263611.3:n.333+2015A=
ENST00000393056.8:c.340-1121A= MANE Select ENSP00000376776.2:n.340-1121A=
ENST00000263611.2:c.297+2015A= ENSP00000263611.2:n.297+2015A=
ENST00000393056.6:c.340-1121A= ENSP00000376776.2:n.340-1121A=
NM_000787.3:c.340-1121A= NP_000778.3:n.340-1121A=
NM_000787.4:c.340-1121A= MANE Select NP_000778.3:n.340-1121A=
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