Canonical Allele Identifier: CA617701387
Gene: SLC30A4 HGNC NCBI

Linked Data

dbSNP Id: rs1432828933
gnomAD v2: 15-45772460-C-T
gnomAD v3: 15-45480262-C-T
gnomAD v4: 15-45480262-C-T
MyVariant Identifiers: chr15:g.45772460C>T (hg19) chr15:g.45480262C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45480262C>T , CM000677.2:g.45480262C>T GRCh38
NC_000015.9:g.45772460C>T , CM000677.1:g.45772460C>T GRCh37
NC_000015.8:g.43559752C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000261867.5:c.*4901G>A MANE Select ENSP00000261867.3:n.*4901G>A
ENST00000261867.4:c.*4901G>A ENSP00000261867.3:n.*4901G>A
NM_013309.5:c.*4901G>A NP_037441.2:n.*4901G>A
NM_013309.6:c.*4901G>A MANE Select NP_037441.2:n.*4901G>A
Search 100 bp 5'
Search 100 bp 3'