Canonical Allele Identifier: CA2174091877
Gene: SLC30A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45480229C= , CM000677.2:g.45480229C= GRCh38
NC_000015.9:g.45772427C= , CM000677.1:g.45772427C= GRCh37
NC_000015.8:g.43559719C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261867.5:c.*4934G= MANE Select ENSP00000261867.3:n.*4934G=
ENST00000261867.4:c.*4934G= ENSP00000261867.3:n.*4934G=
NM_013309.5:c.*4934G= NP_037441.2:n.*4934G=
NM_013309.6:c.*4934G= MANE Select NP_037441.2:n.*4934G=