Canonical Allele Identifier: CA12169037
Gene: SNX18 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

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