Canonical Allele Identifier: CA2202178803
Gene: ABCA17P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2340789C= , CM000678.2:g.2340789C= GRCh38
NC_000016.9:g.2390790C= , CM000678.1:g.2390790C= GRCh37
NC_000016.8:g.2330791C= NCBI36
NG_011790.1:g.4958G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000640929.1:n.42+1458C=
ENST00000512848.5:n.182+1458C=