Canonical Allele Identifier: CA2579501904

Gene: DBH

Linked Data

• dbSNP Id: rs1832157654
• gnomAD v4: 9-133644416-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133644416C>T , CM000671.2:g.133644416C>T	GRCh38
NC_000009.11:g.136509538C>T , CM000671.1:g.136509538C>T	GRCh37
NC_000009.10:g.135499359C>T	NCBI36
NG_008645.1:g.13054C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000393056.8:c.1024+96C>T MANE Select	ENSP00000376776.2:n.1024+96C>T
ENST00000393056.6:c.1024+96C>T	ENSP00000376776.2:n.1024+96C>T
NM_000787.3:c.1024+96C>T	NP_000778.3:n.1024+96C>T
NM_000787.4:c.1024+96C>T MANE Select	NP_000778.3:n.1024+96C>T