Canonical Allele Identifier: CA2202178869
Gene: ABCA17P HGNC NCBI

Linked Data

dbSNP Id: rs2093760481

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2340848A>C , CM000678.2:g.2340848A>C GRCh38
NC_000016.9:g.2390849A>C , CM000678.1:g.2390849A>C GRCh37
NC_000016.8:g.2330850A>C NCBI36
NG_011790.1:g.4899T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000640929.1:n.42+1517A>C
ENST00000512848.5:n.182+1517A>C