Canonical Allele Identifier: CA1547095040
Gene: SNX18 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.54580152T>A , CM000667.2:g.54580152T>A GRCh38
NC_000005.9:g.53875982T>A , CM000667.1:g.53875982T>A GRCh37
NC_000005.8:g.53911739T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017008997.1:c.1622-26251T>A XP_016864486.1:n.1622-26251T>A
XR_001741987.1:n.1816-26251T>A