Canonical Allele Identifier: CA270169448

Gene: SLC30A4

Linked Data

• dbSNP Id: rs1057353653
• gnomAD v3: 15-45480211-T-C
• gnomAD v4: 15-45480211-T-C
• MyVariant Identifiers: chr15:g.45772409T>C (hg19) ; chr15:g.45480211T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.45480211T>C , CM000677.2:g.45480211T>C	GRCh38
NC_000015.9:g.45772409T>C , CM000677.1:g.45772409T>C	GRCh37
NC_000015.8:g.43559701T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000261867.5:c.*4952A>G MANE Select	ENSP00000261867.3:n.*4952A>G
ENST00000261867.4:c.*4952A>G	ENSP00000261867.3:n.*4952A>G
NM_013309.5:c.*4952A>G	NP_037441.2:n.*4952A>G
NM_013309.6:c.*4952A>G MANE Select	NP_037441.2:n.*4952A>G