Canonical Allele Identifier: CA2202178840
Gene: ABCA17P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2340820C= , CM000678.2:g.2340820C= GRCh38
NC_000016.9:g.2390821C= , CM000678.1:g.2390821C= GRCh37
NC_000016.8:g.2330822C= NCBI36
NG_011790.1:g.4927G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000640929.1:n.42+1489C=
ENST00000512848.5:n.182+1489C=