Canonical Allele Identifier: CA719188617
Gene: ABCA17P HGNC NCBI

Linked Data

dbSNP Id: rs1177440053
gnomAD v3: 16-2340839-G-A
gnomAD v4: 16-2340839-G-A
MyVariant Identifiers: chr16:g.2390840G>A (hg19) chr16:g.2340839G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2340839G>A , CM000678.2:g.2340839G>A GRCh38
NC_000016.9:g.2390840G>A , CM000678.1:g.2390840G>A GRCh37
NC_000016.8:g.2330841G>A NCBI36
NG_011790.1:g.4908C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000640929.1:n.42+1508G>A
ENST00000512848.5:n.182+1508G>A
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