Canonical Allele Identifier: CA2628278808
Gene: SLC30A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45480267G>A , CM000677.2:g.45480267G>A GRCh38
NC_000015.9:g.45772465G>A , CM000677.1:g.45772465G>A GRCh37
NC_000015.8:g.43559757G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000261867.5:c.*4896C>T MANE Select ENSP00000261867.3:n.*4896C>T
ENST00000261867.4:c.*4896C>T ENSP00000261867.3:n.*4896C>T
NM_013309.5:c.*4896C>T NP_037441.2:n.*4896C>T
NM_013309.6:c.*4896C>T MANE Select NP_037441.2:n.*4896C>T