Canonical Allele Identifier: CA2628278848
Gene: SLC30A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45480331A>G , CM000677.2:g.45480331A>G GRCh38
NC_000015.9:g.45772529A>G , CM000677.1:g.45772529A>G GRCh37
NC_000015.8:g.43559821A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261867.5:c.*4832T>C MANE Select ENSP00000261867.3:n.*4832T>C
ENST00000261867.4:c.*4832T>C ENSP00000261867.3:n.*4832T>C
NM_013309.5:c.*4832T>C NP_037441.2:n.*4832T>C
NM_013309.6:c.*4832T>C MANE Select NP_037441.2:n.*4832T>C