Canonical Allele Identifier: CA276791249
Gene: ABCA17P HGNC NCBI

Linked Data

dbSNP Id: rs982374033
MyVariant Identifiers: chr16:g.2390905C>T (hg19) chr16:g.2340904C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2340904C>T , CM000678.2:g.2340904C>T GRCh38
NC_000016.9:g.2390905C>T , CM000678.1:g.2390905C>T GRCh37
NC_000016.8:g.2330906C>T NCBI36
NG_011790.1:g.4843G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000640929.1:n.42+1573C>T
ENST00000512848.5:n.182+1573C>T
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