Canonical Allele Identifier: CA200954200

Gene: DBH

Linked Data

• dbSNP Id: rs1009126881
• gnomAD v2: 9-136503759-G-T
• gnomAD v3: 9-133638637-G-T
• gnomAD v4: 9-133638637-G-T
• MyVariant Identifiers: chr9:g.136503759G>T (hg19) ; chr9:g.133638637G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133638637G>T , CM000671.2:g.133638637G>T	GRCh38
NC_000009.11:g.136503759G>T , CM000671.1:g.136503759G>T	GRCh37
NC_000009.10:g.135493580G>T	NCBI36
NG_008645.1:g.7275G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263611.3:c.333+1927G>T	ENSP00000263611.3:n.333+1927G>T
ENST00000393056.8:c.340-1209G>T MANE Select	ENSP00000376776.2:n.340-1209G>T
ENST00000263611.2:c.297+1927G>T	ENSP00000263611.2:n.297+1927G>T
ENST00000393056.6:c.340-1209G>T	ENSP00000376776.2:n.340-1209G>T
NM_000787.3:c.340-1209G>T	NP_000778.3:n.340-1209G>T
NM_000787.4:c.340-1209G>T MANE Select	NP_000778.3:n.340-1209G>T