Canonical Allele Identifier: CA2174091848
Gene: SLC30A4 HGNC NCBI

Linked Data

dbSNP Id: rs1891582695
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45480149A>C , CM000677.2:g.45480149A>C GRCh38
NC_000015.9:g.45772347A>C , CM000677.1:g.45772347A>C GRCh37
NC_000015.8:g.43559639A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261867.5:c.*5014T>G MANE Select ENSP00000261867.3:n.*5014T>G
ENST00000261867.4:c.*5014T>G ENSP00000261867.3:n.*5014T>G
NM_013309.5:c.*5014T>G NP_037441.2:n.*5014T>G
NM_013309.6:c.*5014T>G MANE Select NP_037441.2:n.*5014T>G
Search 100 bp 5'
Search 100 bp 3'