Canonical Allele Identifier: CA2202178771
Gene: ABCA17P HGNC NCBI

Linked Data

dbSNP Id: rs2093759945

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2340764_2340765insT , CM000678.2:g.2340764_2340765insT GRCh38
NC_000016.9:g.2390765_2390766insT , CM000678.1:g.2390765_2390766insT GRCh37
NC_000016.8:g.2330766_2330767insT NCBI36
NG_011790.1:g.4982_4983insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000640929.1:n.42+1433_42+1434insT
ENST00000512848.5:n.182+1433_182+1434insT