Canonical Allele Identifier: CA620708666
Gene: ABCA17P HGNC NCBI

Linked Data

dbSNP Id: rs1308777040 rs2141730447
gnomAD v2: 16-2390877-A-G
gnomAD v3: 16-2340876-A-G
gnomAD v4: 16-2340876-A-G
MyVariant Identifiers: chr16:g.2390877A>G (hg19) chr16:g.2340876A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2340876A>G , CM000678.2:g.2340876A>G GRCh38
NC_000016.9:g.2390877A>G , CM000678.1:g.2390877A>G GRCh37
NC_000016.8:g.2330878A>G NCBI36
NG_011790.1:g.4871T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000640929.1:n.42+1545A>G
ENST00000512848.5:n.182+1545A>G
Search 100 bp 5'
Search 100 bp 3'