Canonical Allele Identifier: CA2174091919
Gene: SLC30A4 HGNC NCBI

Linked Data

dbSNP Id: rs1595518813
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45480339C>A , CM000677.2:g.45480339C>A GRCh38
NC_000015.9:g.45772537C>A , CM000677.1:g.45772537C>A GRCh37
NC_000015.8:g.43559829C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000261867.5:c.*4824G>T MANE Select ENSP00000261867.3:n.*4824G>T
ENST00000261867.4:c.*4824G>T ENSP00000261867.3:n.*4824G>T
NM_013309.5:c.*4824G>T NP_037441.2:n.*4824G>T
NM_013309.6:c.*4824G>T MANE Select NP_037441.2:n.*4824G>T
Search 100 bp 5'
Search 100 bp 3'