Canonical Allele Identifier: CA1882770196
Gene: DBH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133638697T= , CM000671.2:g.133638697T= GRCh38
NC_000009.11:g.136503819T= , CM000671.1:g.136503819T= GRCh37
NC_000009.10:g.135493640T= NCBI36
NG_008645.1:g.7335T=

Transcript Alleles

HGVS Amino-acid change
ENST00000263611.3:c.333+1987T= ENSP00000263611.3:n.333+1987T=
ENST00000393056.8:c.340-1149T= MANE Select ENSP00000376776.2:n.340-1149T=
ENST00000263611.2:c.297+1987T= ENSP00000263611.2:n.297+1987T=
ENST00000393056.6:c.340-1149T= ENSP00000376776.2:n.340-1149T=
NM_000787.3:c.340-1149T= NP_000778.3:n.340-1149T=
NM_000787.4:c.340-1149T= MANE Select NP_000778.3:n.340-1149T=
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