Canonical Allele Identifier: CA2631192803
Gene: ABCA17P HGNC NCBI

Linked Data

gnomAD v4: 16-2340780-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2340780G>A , CM000678.2:g.2340780G>A GRCh38
NC_000016.9:g.2390781G>A , CM000678.1:g.2390781G>A GRCh37
NC_000016.8:g.2330782G>A NCBI36
NG_011790.1:g.4967C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000640929.1:n.42+1449G>A
ENST00000512848.5:n.182+1449G>A