Canonical Allele Identifier: CA858831647
Gene: SNX30 HGNC NCBI

Linked Data

dbSNP Id: rs1324271354
MyVariant Identifiers: chr9:g.115550441T>C (hg19) chr9:g.112788161T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.112788161T>C , CM000671.2:g.112788161T>C GRCh38
NC_000009.11:g.115550441T>C , CM000671.1:g.115550441T>C GRCh37
NC_000009.10:g.114590262T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000374232.8:c.157-16615T>C MANE Select ENSP00000363349.3:n.157-16615T>C
ENST00000374232.7:c.157-16615T>C ENSP00000363349.3:n.157-16615T>C
NM_001012994.1:c.157-16615T>C NP_001013012.1:n.157-16615T>C
XM_005251986.3:c.-156-16615T>C XP_005252043.1:n.-156-16615T>C
XM_011518691.1:c.157-16615T>C XP_011516993.1:n.157-16615T>C
XM_011518691.2:c.157-16615T>C XP_011516993.1:n.157-16615T>C
XM_017014716.2:c.34-16615T>C XP_016870205.1:n.34-16615T>C
XM_024447544.1:c.-156-16615T>C XP_024303312.1:n.-156-16615T>C
NM_001012994.2:c.157-16615T>C MANE Select NP_001013012.1:n.157-16615T>C
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