Canonical Allele Identifier: CA2692393560
Gene: DBH HGNC NCBI

Linked Data

gnomAD v4: 9-133644414-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133644414T>C , CM000671.2:g.133644414T>C GRCh38
NC_000009.11:g.136509536T>C , CM000671.1:g.136509536T>C GRCh37
NC_000009.10:g.135499357T>C NCBI36
NG_008645.1:g.13052T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000393056.8:c.1024+94T>C MANE Select ENSP00000376776.2:n.1024+94T>C
ENST00000393056.6:c.1024+94T>C ENSP00000376776.2:n.1024+94T>C
NM_000787.3:c.1024+94T>C NP_000778.3:n.1024+94T>C
NM_000787.4:c.1024+94T>C MANE Select NP_000778.3:n.1024+94T>C
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