Canonical Allele Identifier: CA2202178891
Gene: ABCA17P HGNC NCBI

Linked Data

dbSNP Id: rs2141730461

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2340879T>A , CM000678.2:g.2340879T>A GRCh38
NC_000016.9:g.2390880T>A , CM000678.1:g.2390880T>A GRCh37
NC_000016.8:g.2330881T>A NCBI36
NG_011790.1:g.4868A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000640929.1:n.42+1548T>A
ENST00000512848.5:n.182+1548T>A