Canonical Allele Identifier: CA2174091902
Gene: SLC30A4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45480289T= , CM000677.2:g.45480289T= GRCh38
NC_000015.9:g.45772487T= , CM000677.1:g.45772487T= GRCh37
NC_000015.8:g.43559779T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261867.5:c.*4874A= MANE Select ENSP00000261867.3:n.*4874A=
ENST00000261867.4:c.*4874A= ENSP00000261867.3:n.*4874A=
NM_013309.5:c.*4874A= NP_037441.2:n.*4874A=
NM_013309.6:c.*4874A= MANE Select NP_037441.2:n.*4874A=
Search 100 bp 5'
Search 100 bp 3'