Canonical Allele Identifier: CA2628278792
Gene: SLC30A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45480254C>A , CM000677.2:g.45480254C>A GRCh38
NC_000015.9:g.45772452C>A , CM000677.1:g.45772452C>A GRCh37
NC_000015.8:g.43559744C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000261867.5:c.*4909G>T MANE Select ENSP00000261867.3:n.*4909G>T
ENST00000261867.4:c.*4909G>T ENSP00000261867.3:n.*4909G>T
NM_013309.5:c.*4909G>T NP_037441.2:n.*4909G>T
NM_013309.6:c.*4909G>T MANE Select NP_037441.2:n.*4909G>T