Canonical Allele Identifier: CA713150330
Gene: SLC30A4 HGNC NCBI

Linked Data

dbSNP Id: rs1380804944

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45480336C>T , CM000677.2:g.45480336C>T GRCh38
NC_000015.9:g.45772534C>T , CM000677.1:g.45772534C>T GRCh37
NC_000015.8:g.43559826C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261867.5:c.*4827G>A MANE Select ENSP00000261867.3:n.*4827G>A
ENST00000261867.4:c.*4827G>A ENSP00000261867.3:n.*4827G>A
NM_013309.5:c.*4827G>A NP_037441.2:n.*4827G>A
NM_013309.6:c.*4827G>A MANE Select NP_037441.2:n.*4827G>A