Canonical Allele Identifier: CA2628278849
Gene: SLC30A4 HGNC NCBI

Linked Data

gnomAD v4: 15-45480338-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45480338T>A , CM000677.2:g.45480338T>A GRCh38
NC_000015.9:g.45772536T>A , CM000677.1:g.45772536T>A GRCh37
NC_000015.8:g.43559828T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000261867.5:c.*4825A>T MANE Select ENSP00000261867.3:n.*4825A>T
ENST00000261867.4:c.*4825A>T ENSP00000261867.3:n.*4825A>T
NM_013309.5:c.*4825A>T NP_037441.2:n.*4825A>T
NM_013309.6:c.*4825A>T MANE Select NP_037441.2:n.*4825A>T
Search 100 bp 5'
Search 100 bp 3'