Canonical Allele Identifier: CA2692393559

Gene: DBH

Linked Data

• gnomAD v4: 9-133644412-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133644412G>T , CM000671.2:g.133644412G>T	GRCh38
NC_000009.11:g.136509534G>T , CM000671.1:g.136509534G>T	GRCh37
NC_000009.10:g.135499355G>T	NCBI36
NG_008645.1:g.13050G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393056.8:c.1024+92G>T MANE Select	ENSP00000376776.2:n.1024+92G>T
ENST00000393056.6:c.1024+92G>T	ENSP00000376776.2:n.1024+92G>T
NM_000787.3:c.1024+92G>T	NP_000778.3:n.1024+92G>T
NM_000787.4:c.1024+92G>T MANE Select	NP_000778.3:n.1024+92G>T