Canonical Allele Identifier: CA1410143265
Gene: CPHL1P HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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