Canonical Allele Identifier: CA2631192886
Gene: ABCA17P HGNC NCBI

Linked Data

gnomAD v4: 16-2340897-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2340897G>T , CM000678.2:g.2340897G>T GRCh38
NC_000016.9:g.2390898G>T , CM000678.1:g.2390898G>T GRCh37
NC_000016.8:g.2330899G>T NCBI36
NG_011790.1:g.4850C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000640929.1:n.42+1566G>T
ENST00000512848.5:n.182+1566G>T