Canonical Allele Identifier: CA1139342324
Gene: ANOS2P HGNC NCBI

Linked Data

gnomAD v3: Y-13787217-C-T
gnomAD v4: Y-13787217-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.13787217C>T , CM000686.2:g.13787217C>T GRCh38
NC_000024.9:g.15899097C>T , CM000686.1:g.15899097C>T GRCh37
NC_000024.8:g.14408491C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000652544.1:n.684+32428C>T
ENST00000430079.5:n.430-3702C>T
ENST00000460561.1:n.213-3702C>T
ENST00000472227.5:n.351-3702C>T