Canonical Allele Identifier: CA2631192867
Gene: ABCA17P HGNC NCBI

Linked Data

gnomAD v4: 16-2340867-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2340867G>A , CM000678.2:g.2340867G>A GRCh38
NC_000016.9:g.2390868G>A , CM000678.1:g.2390868G>A GRCh37
NC_000016.8:g.2330869G>A NCBI36
NG_011790.1:g.4880C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000640929.1:n.42+1536G>A
ENST00000512848.5:n.182+1536G>A