Canonical Allele Identifier: CA2803988242
Gene: SLC30A4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45480266A>G , CM000677.2:g.45480266A>G GRCh38
NC_000015.9:g.45772464A>G , CM000677.1:g.45772464A>G GRCh37
NC_000015.8:g.43559756A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000261867.5:c.*4897T>C MANE Select ENSP00000261867.3:n.*4897T>C
ENST00000261867.4:c.*4897T>C ENSP00000261867.3:n.*4897T>C
NM_013309.5:c.*4897T>C NP_037441.2:n.*4897T>C
NM_013309.6:c.*4897T>C MANE Select NP_037441.2:n.*4897T>C