Canonical Allele Identifier: CA12129984

Gene: SNX18

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.54606509G>A , CM000667.2:g.54606509G>A	GRCh38
NC_000005.9:g.53902339G>A , CM000667.1:g.53902339G>A	GRCh37
NC_000005.8:g.53938096G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_017008997.1:c.*102G>A	XP_016864486.1:n.*102G>A
XR_001741987.1:n.1919+3G>A