Canonical Allele Identifier: CA1547095042
Community Standard Title: NC_000005.10:g.54580152T=
Gene: SNX18 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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