Canonical Allele Identifier: CA2174091905

Gene: SLC30A4

Linked Data

• dbSNP Id: rs1891584768

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.45480301A>G , CM000677.2:g.45480301A>G	GRCh38
NC_000015.9:g.45772499A>G , CM000677.1:g.45772499A>G	GRCh37
NC_000015.8:g.43559791A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261867.5:c.*4862T>C MANE Select	ENSP00000261867.3:n.*4862T>C
ENST00000261867.4:c.*4862T>C	ENSP00000261867.3:n.*4862T>C
NM_013309.5:c.*4862T>C	NP_037441.2:n.*4862T>C
NM_013309.6:c.*4862T>C MANE Select	NP_037441.2:n.*4862T>C