Canonical Allele Identifier: CA973792084
Gene: ABCA17P HGNC NCBI

Linked Data

dbSNP Id: rs2093760379
gnomAD v3: 16-2340825-G-T
gnomAD v4: 16-2340825-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2340825G>T , CM000678.2:g.2340825G>T GRCh38
NC_000016.9:g.2390826G>T , CM000678.1:g.2390826G>T GRCh37
NC_000016.8:g.2330827G>T NCBI36
NG_011790.1:g.4922C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000640929.1:n.42+1494G>T
ENST00000512848.5:n.182+1494G>T