Canonical Allele Identifier: CA2202178850
Gene: ABCA17P HGNC NCBI

Linked Data

gnomAD v4: 16-2340831-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2340831G>A , CM000678.2:g.2340831G>A GRCh38
NC_000016.9:g.2390832G>A , CM000678.1:g.2390832G>A GRCh37
NC_000016.8:g.2330833G>A NCBI36
NG_011790.1:g.4916C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000640929.1:n.42+1500G>A
ENST00000512848.5:n.182+1500G>A