Canonical Allele Identifier: CA617701389
Gene: SLC30A4 HGNC NCBI

Linked Data

dbSNP Id: rs1358726736
gnomAD v2: 15-45772536-T-C
gnomAD v3: 15-45480338-T-C
gnomAD v4: 15-45480338-T-C
MyVariant Identifiers: chr15:g.45772536T>C (hg19) chr15:g.45480338T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45480338T>C , CM000677.2:g.45480338T>C GRCh38
NC_000015.9:g.45772536T>C , CM000677.1:g.45772536T>C GRCh37
NC_000015.8:g.43559828T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000261867.5:c.*4825A>G MANE Select ENSP00000261867.3:n.*4825A>G
ENST00000261867.4:c.*4825A>G ENSP00000261867.3:n.*4825A>G
NM_013309.5:c.*4825A>G NP_037441.2:n.*4825A>G
NM_013309.6:c.*4825A>G MANE Select NP_037441.2:n.*4825A>G
Search 100 bp 5'
Search 100 bp 3'