Canonical Allele Identifier: CA2202178782
Gene: ABCA17P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2340771G= , CM000678.2:g.2340771G= GRCh38
NC_000016.9:g.2390772G= , CM000678.1:g.2390772G= GRCh37
NC_000016.8:g.2330773G= NCBI36
NG_011790.1:g.4976C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000640929.1:n.42+1440G=
ENST00000512848.5:n.182+1440G=