Canonical Allele Identifier: CA2174091895
Gene: SLC30A4 HGNC NCBI

Linked Data

dbSNP Id: rs1891584489
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45480272C>T , CM000677.2:g.45480272C>T GRCh38
NC_000015.9:g.45772470C>T , CM000677.1:g.45772470C>T GRCh37
NC_000015.8:g.43559762C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000261867.5:c.*4891G>A MANE Select ENSP00000261867.3:n.*4891G>A
ENST00000261867.4:c.*4891G>A ENSP00000261867.3:n.*4891G>A
NM_013309.5:c.*4891G>A NP_037441.2:n.*4891G>A
NM_013309.6:c.*4891G>A MANE Select NP_037441.2:n.*4891G>A
Search 100 bp 5'
Search 100 bp 3'