Canonical Allele Identifier: CA2202178897
Gene: ABCA17P HGNC NCBI

Linked Data

dbSNP Id: rs2093760598
gnomAD v4: 16-2340884-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2340884C>T , CM000678.2:g.2340884C>T GRCh38
NC_000016.9:g.2390885C>T , CM000678.1:g.2390885C>T GRCh37
NC_000016.8:g.2330886C>T NCBI36
NG_011790.1:g.4863G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000640929.1:n.42+1553C>T
ENST00000512848.5:n.182+1553C>T