Canonical Allele Identifier: CA2803988240
Gene: SLC30A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45480224T>C , CM000677.2:g.45480224T>C GRCh38
NC_000015.9:g.45772422T>C , CM000677.1:g.45772422T>C GRCh37
NC_000015.8:g.43559714T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000261867.5:c.*4939A>G MANE Select ENSP00000261867.3:n.*4939A>G
ENST00000261867.4:c.*4939A>G ENSP00000261867.3:n.*4939A>G
NM_013309.5:c.*4939A>G NP_037441.2:n.*4939A>G
NM_013309.6:c.*4939A>G MANE Select NP_037441.2:n.*4939A>G