Canonical Allele Identifier: CA2202178898
Gene: ABCA17P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2340885A= , CM000678.2:g.2340885A= GRCh38
NC_000016.9:g.2390886A= , CM000678.1:g.2390886A= GRCh37
NC_000016.8:g.2330887A= NCBI36
NG_011790.1:g.4862T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000640929.1:n.42+1554A=
ENST00000512848.5:n.182+1554A=