Canonical Allele Identifier: CA270169507
Gene: SLC30A4 HGNC NCBI

Linked Data

dbSNP Id: rs28404754
MyVariant Identifiers: chr15:g.45772531G>C (hg19) chr15:g.45480333G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45480333G>C , CM000677.2:g.45480333G>C GRCh38
NC_000015.9:g.45772531G>C , CM000677.1:g.45772531G>C GRCh37
NC_000015.8:g.43559823G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261867.5:c.*4830C>G MANE Select ENSP00000261867.3:n.*4830C>G
ENST00000261867.4:c.*4830C>G ENSP00000261867.3:n.*4830C>G
NM_013309.5:c.*4830C>G NP_037441.2:n.*4830C>G
NM_013309.6:c.*4830C>G MANE Select NP_037441.2:n.*4830C>G
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