Canonical Allele Identifier: CA973792138
Gene: ABCA17P HGNC NCBI

Linked Data

dbSNP Id: rs2093760613

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2340886T>G , CM000678.2:g.2340886T>G GRCh38
NC_000016.9:g.2390887T>G , CM000678.1:g.2390887T>G GRCh37
NC_000016.8:g.2330888T>G NCBI36
NG_011790.1:g.4861A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000640929.1:n.42+1555T>G
ENST00000512848.5:n.182+1555T>G