Canonical Allele Identifier: CA2202178871
Gene: ABCA17P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2340854G= , CM000678.2:g.2340854G= GRCh38
NC_000016.9:g.2390855G= , CM000678.1:g.2390855G= GRCh37
NC_000016.8:g.2330856G= NCBI36
NG_011790.1:g.4893C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000640929.1:n.42+1523G=
ENST00000512848.5:n.182+1523G=