Canonical Allele Identifier: CA11513465
Gene: CPHL1P HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.149259527A>G , CM000665.2:g.149259527A>G GRCh38
NC_000003.11:g.148977314A>G , CM000665.1:g.148977314A>G GRCh37
NC_000003.10:g.150460004A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000461341.2:n.1210-1938T>C
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