Canonical Allele Identifier: CA200957458
Gene: DBH HGNC NCBI

Linked Data

dbSNP Id: rs927771913
MyVariant Identifiers: chr9:g.136503846T>C (hg19) chr9:g.133638724T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133638724T>C , CM000671.2:g.133638724T>C GRCh38
NC_000009.11:g.136503846T>C , CM000671.1:g.136503846T>C GRCh37
NC_000009.10:g.135493667T>C NCBI36
NG_008645.1:g.7362T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000263611.3:c.333+2014T>C ENSP00000263611.3:n.333+2014T>C
ENST00000393056.8:c.340-1122T>C MANE Select ENSP00000376776.2:n.340-1122T>C
ENST00000263611.2:c.297+2014T>C ENSP00000263611.2:n.297+2014T>C
ENST00000393056.6:c.340-1122T>C ENSP00000376776.2:n.340-1122T>C
NM_000787.3:c.340-1122T>C NP_000778.3:n.340-1122T>C
NM_000787.4:c.340-1122T>C MANE Select NP_000778.3:n.340-1122T>C
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