Canonical Allele Identifier: CA2202178802
Gene: ABCA17P HGNC NCBI

Linked Data

dbSNP Id: rs2093760155
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2340786A>C , CM000678.2:g.2340786A>C GRCh38
NC_000016.9:g.2390787A>C , CM000678.1:g.2390787A>C GRCh37
NC_000016.8:g.2330788A>C NCBI36
NG_011790.1:g.4961T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000640929.1:n.42+1455A>C
ENST00000512848.5:n.182+1455A>C
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