Canonical Allele Identifier: CA590259936
Gene: SNX30 HGNC NCBI

Linked Data

dbSNP Id: rs1406382768
gnomAD v2: 9-115550392-G-A
gnomAD v3: 9-112788112-G-A
gnomAD v4: 9-112788112-G-A
MyVariant Identifiers: chr9:g.115550392G>A (hg19) chr9:g.112788112G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.112788112G>A , CM000671.2:g.112788112G>A GRCh38
NC_000009.11:g.115550392G>A , CM000671.1:g.115550392G>A GRCh37
NC_000009.10:g.114590213G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000374232.8:c.157-16664G>A MANE Select ENSP00000363349.3:n.157-16664G>A
ENST00000374232.7:c.157-16664G>A ENSP00000363349.3:n.157-16664G>A
NM_001012994.1:c.157-16664G>A NP_001013012.1:n.157-16664G>A
XM_005251986.3:c.-156-16664G>A XP_005252043.1:n.-156-16664G>A
XM_011518691.1:c.157-16664G>A XP_011516993.1:n.157-16664G>A
XM_011518691.2:c.157-16664G>A XP_011516993.1:n.157-16664G>A
XM_017014716.2:c.34-16664G>A XP_016870205.1:n.34-16664G>A
XM_024447544.1:c.-156-16664G>A XP_024303312.1:n.-156-16664G>A
NM_001012994.2:c.157-16664G>A MANE Select NP_001013012.1:n.157-16664G>A
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