Canonical Allele Identifier: CA198850734

Gene: SNX30

Linked Data

• dbSNP Id: rs787274
• gnomAD v2: 9-115550363-A-C
• gnomAD v3: 9-112788083-A-C
• gnomAD v4: 9-112788083-A-C
• MyVariant Identifiers: chr9:g.115550363A>C (hg19) ; chr9:g.112788083A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.112788083A>C , CM000671.2:g.112788083A>C	GRCh38
NC_000009.11:g.115550363A>C , CM000671.1:g.115550363A>C	GRCh37
NC_000009.10:g.114590184A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000374232.8:c.157-16693A>C MANE Select	ENSP00000363349.3:n.157-16693A>C
ENST00000374232.7:c.157-16693A>C	ENSP00000363349.3:n.157-16693A>C
NM_001012994.1:c.157-16693A>C	NP_001013012.1:n.157-16693A>C
XM_005251986.3:c.-156-16693A>C	XP_005252043.1:n.-156-16693A>C
XM_011518691.1:c.157-16693A>C	XP_011516993.1:n.157-16693A>C
XM_011518691.2:c.157-16693A>C	XP_011516993.1:n.157-16693A>C
XM_017014716.2:c.34-16693A>C	XP_016870205.1:n.34-16693A>C
XM_024447544.1:c.-156-16693A>C	XP_024303312.1:n.-156-16693A>C
NM_001012994.2:c.157-16693A>C MANE Select	NP_001013012.1:n.157-16693A>C