Canonical Allele Identifier: CA812172575
Gene: SNX18 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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