Canonical Allele Identifier: CA2631192815
Gene: ABCA17P HGNC NCBI

Linked Data

gnomAD v4: 16-2340802-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2340802A>G , CM000678.2:g.2340802A>G GRCh38
NC_000016.9:g.2390803A>G , CM000678.1:g.2390803A>G GRCh37
NC_000016.8:g.2330804A>G NCBI36
NG_011790.1:g.4945T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000640929.1:n.42+1471A>G
ENST00000512848.5:n.182+1471A>G