Canonical Allele Identifier: CA858831645

Gene: SNX30

Linked Data

• dbSNP Id: rs1271735903
• gnomAD v3: 9-112788153-A-G
• gnomAD v4: 9-112788153-A-G
• MyVariant Identifiers: chr9:g.115550433A>G (hg19) ; chr9:g.112788153A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.112788153A>G , CM000671.2:g.112788153A>G	GRCh38
NC_000009.11:g.115550433A>G , CM000671.1:g.115550433A>G	GRCh37
NC_000009.10:g.114590254A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374232.8:c.157-16623A>G MANE Select	ENSP00000363349.3:n.157-16623A>G
ENST00000374232.7:c.157-16623A>G	ENSP00000363349.3:n.157-16623A>G
NM_001012994.1:c.157-16623A>G	NP_001013012.1:n.157-16623A>G
XM_005251986.3:c.-156-16623A>G	XP_005252043.1:n.-156-16623A>G
XM_011518691.1:c.157-16623A>G	XP_011516993.1:n.157-16623A>G
XM_011518691.2:c.157-16623A>G	XP_011516993.1:n.157-16623A>G
XM_017014716.2:c.34-16623A>G	XP_016870205.1:n.34-16623A>G
XM_024447544.1:c.-156-16623A>G	XP_024303312.1:n.-156-16623A>G
NM_001012994.2:c.157-16623A>G MANE Select	NP_001013012.1:n.157-16623A>G