Canonical Allele Identifier: CA270169467
Gene: SLC30A4 HGNC NCBI

Linked Data

dbSNP Id: rs894653469
gnomAD v2: 15-45772435-A-G
gnomAD v3: 15-45480237-A-G
gnomAD v4: 15-45480237-A-G
MyVariant Identifiers: chr15:g.45772435A>G (hg19) chr15:g.45480237A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45480237A>G , CM000677.2:g.45480237A>G GRCh38
NC_000015.9:g.45772435A>G , CM000677.1:g.45772435A>G GRCh37
NC_000015.8:g.43559727A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000261867.5:c.*4926T>C MANE Select ENSP00000261867.3:n.*4926T>C
ENST00000261867.4:c.*4926T>C ENSP00000261867.3:n.*4926T>C
NM_013309.5:c.*4926T>C NP_037441.2:n.*4926T>C
NM_013309.6:c.*4926T>C MANE Select NP_037441.2:n.*4926T>C
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