Canonical Allele Identifier: CA1139339438
Gene: ANOS2P HGNC NCBI

Linked Data

gnomAD v3: Y-13765645-C-T
gnomAD v4: Y-13765645-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.13765645C>T , CM000686.2:g.13765645C>T GRCh38
NC_000024.9:g.15877525C>T , CM000686.1:g.15877525C>T GRCh37
NC_000024.8:g.14386919C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000652544.1:n.684+10856C>T
ENST00000430079.5:n.429+10856C>T
ENST00000460561.1:n.212+10856C>T
ENST00000472227.5:n.350+13640C>T
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