Canonical Allele Identifier: CA969344911
Gene: SLC30A4 HGNC NCBI

Linked Data

dbSNP Id: rs1566872510
gnomAD v3: 15-45480131-G-A
gnomAD v4: 15-45480131-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45480131G>A , CM000677.2:g.45480131G>A GRCh38
NC_000015.9:g.45772329G>A , CM000677.1:g.45772329G>A GRCh37
NC_000015.8:g.43559621G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261867.5:c.*5032C>T MANE Select ENSP00000261867.3:n.*5032C>T
ENST00000261867.4:c.*5032C>T ENSP00000261867.3:n.*5032C>T
NM_013309.5:c.*5032C>T NP_037441.2:n.*5032C>T
NM_013309.6:c.*5032C>T MANE Select NP_037441.2:n.*5032C>T
Search 100 bp 5'
Search 100 bp 3'