Canonical Allele Identifier: CA2631192858
Gene: ABCA17P HGNC NCBI

Linked Data

gnomAD v4: 16-2340859-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2340859T>C , CM000678.2:g.2340859T>C GRCh38
NC_000016.9:g.2390860T>C , CM000678.1:g.2390860T>C GRCh37
NC_000016.8:g.2330861T>C NCBI36
NG_011790.1:g.4888A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000640929.1:n.42+1528T>C
ENST00000512848.5:n.182+1528T>C
Search 100 bp 5'
Search 100 bp 3'