Canonical Allele Identifier: CA2579501751
Gene: DBH HGNC NCBI

Linked Data

gnomAD v4: 9-133636732-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133636732G>C , CM000671.2:g.133636732G>C GRCh38
NC_000009.11:g.136501854G>C , CM000671.1:g.136501854G>C GRCh37
NC_000009.10:g.135491675G>C NCBI36
NG_008645.1:g.5370G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000263611.3:c.333+22G>C ENSP00000263611.3:n.333+22G>C
ENST00000393056.8:c.339+22G>C MANE Select ENSP00000376776.2:n.339+22G>C
ENST00000263611.2:c.297+22G>C ENSP00000263611.2:n.297+22G>C
ENST00000393056.6:c.339+22G>C ENSP00000376776.2:n.339+22G>C
NM_000787.3:c.339+22G>C NP_000778.3:n.339+22G>C
NM_000787.4:c.339+22G>C MANE Select NP_000778.3:n.339+22G>C
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