Canonical Allele Identifier: CA1139342305
Gene: ANOS2P HGNC NCBI

Linked Data

gnomAD v3: Y-13787176-T-A
gnomAD v4: Y-13787176-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.13787176T>A , CM000686.2:g.13787176T>A GRCh38
NC_000024.9:g.15899056T>A , CM000686.1:g.15899056T>A GRCh37
NC_000024.8:g.14408450T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000652544.1:n.684+32387T>A
ENST00000430079.5:n.430-3743T>A
ENST00000460561.1:n.213-3743T>A
ENST00000472227.5:n.351-3743T>A
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