Canonical Allele Identifier: CA1882777169

Gene: DBH

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133644188_133644192delinsCCCGT , CM000671.2:g.133644188_133644192delinsCCCGT	GRCh38
NC_000009.11:g.136509310_136509314delinsCCCGT , CM000671.1:g.136509310_136509314delinsCCCGT	GRCh37
NC_000009.10:g.135499131_135499135delinsCCCGT	NCBI36
NG_008645.1:g.12826_12830delinsCCCGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393056.8:c.922-30_922-26delinsCCCGT MANE Select	ENSP00000376776.2:n.922-30_922-26delinsCCCGT
ENST00000393056.6:c.922-30_922-26delinsCCCGT	ENSP00000376776.2:n.922-30_922-26delinsCCCGT
NM_000787.3:c.922-30_922-26delinsCCCGT	NP_000778.3:n.922-30_922-26delinsCCCGT
NM_000787.4:c.922-30_922-26delinsCCCGT MANE Select	NP_000778.3:n.922-30_922-26delinsCCCGT