Canonical Allele Identifier: CA2670470470
Gene: SLC30A9 HGNC NCBI

Linked Data

gnomAD v4: 4-42001554-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42001554G>T , CM000666.2:g.42001554G>T GRCh38
NC_000004.11:g.42003571G>T , CM000666.1:g.42003571G>T GRCh37
NC_000004.10:g.41698328G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264451.12:c.110-62G>T MANE Select ENSP00000264451.6:n.110-62G>T
ENST00000264451.11:c.110-62G>T ENSP00000264451.6:n.110-62G>T
ENST00000510460.1:n.235-62G>T
ENST00000513699.5:c.110-62G>T ENSP00000423529.1:n.110-62G>T
NM_006345.3:c.110-62G>T NP_006336.3:n.110-62G>T
XM_011513620.1:c.110-62G>T XP_011511922.1:n.110-62G>T
XM_017007654.2:c.110-62G>T XP_016863143.1:n.110-62G>T
XR_001741095.2:n.260-62G>T
NM_006345.4:c.110-62G>T MANE Select NP_006336.3:n.110-62G>T