Canonical Allele Identifier: CA1139347757
Gene: ANOS2P HGNC NCBI

Linked Data

gnomAD v3: Y-13836272-T-C
gnomAD v4: Y-13836272-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.13836272T>C , CM000686.2:g.13836272T>C GRCh38
NC_000024.9:g.15948152T>C , CM000686.1:g.15948152T>C GRCh37
NC_000024.8:g.14457546T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000652544.1:n.685-22245T>C
ENST00000430079.5:n.478-18172T>C
ENST00000460561.1:n.261-22245T>C
ENST00000472227.5:n.399-22230T>C
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