Canonical Allele Identifier: CA2631192838
Gene: ABCA17P HGNC NCBI

Linked Data

gnomAD v4: 16-2340834-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2340834G>T , CM000678.2:g.2340834G>T GRCh38
NC_000016.9:g.2390835G>T , CM000678.1:g.2390835G>T GRCh37
NC_000016.8:g.2330836G>T NCBI36
NG_011790.1:g.4913C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000640929.1:n.42+1503G>T
ENST00000512848.5:n.182+1503G>T
Search 100 bp 5'
Search 100 bp 3'