Canonical Allele Identifier: CA2202178800
Gene: ABCA17P HGNC NCBI

Linked Data

dbSNP Id: rs2093760150
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2340785C>T , CM000678.2:g.2340785C>T GRCh38
NC_000016.9:g.2390786C>T , CM000678.1:g.2390786C>T GRCh37
NC_000016.8:g.2330787C>T NCBI36
NG_011790.1:g.4962G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000640929.1:n.42+1454C>T
ENST00000512848.5:n.182+1454C>T
Search 100 bp 5'
Search 100 bp 3'