Canonical Allele Identifier: CA2628278832
Gene: SLC30A4 HGNC NCBI

Linked Data

gnomAD v4: 15-45480315-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45480315T>C , CM000677.2:g.45480315T>C GRCh38
NC_000015.9:g.45772513T>C , CM000677.1:g.45772513T>C GRCh37
NC_000015.8:g.43559805T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261867.5:c.*4848A>G MANE Select ENSP00000261867.3:n.*4848A>G
ENST00000261867.4:c.*4848A>G ENSP00000261867.3:n.*4848A>G
NM_013309.5:c.*4848A>G NP_037441.2:n.*4848A>G
NM_013309.6:c.*4848A>G MANE Select NP_037441.2:n.*4848A>G
Search 100 bp 5'
Search 100 bp 3'