Canonical Allele Identifier: CA270169495
Gene: SLC30A4 HGNC NCBI

Linked Data

dbSNP Id: rs753807846
gnomAD v2: 15-45772506-T-C
gnomAD v3: 15-45480308-T-C
gnomAD v4: 15-45480308-T-C
MyVariant Identifiers: chr15:g.45772506T>C (hg19) chr15:g.45480308T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.45480308T>C , CM000677.2:g.45480308T>C GRCh38
NC_000015.9:g.45772506T>C , CM000677.1:g.45772506T>C GRCh37
NC_000015.8:g.43559798T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261867.5:c.*4855A>G MANE Select ENSP00000261867.3:n.*4855A>G
ENST00000261867.4:c.*4855A>G ENSP00000261867.3:n.*4855A>G
NM_013309.5:c.*4855A>G NP_037441.2:n.*4855A>G
NM_013309.6:c.*4855A>G MANE Select NP_037441.2:n.*4855A>G
Search 100 bp 5'
Search 100 bp 3'