Canonical Allele Identifier: CA1139347778
Gene: ANOS2P HGNC NCBI

Linked Data

dbSNP Id: rs2079820436
gnomAD v3: Y-13836470-G-A
gnomAD v4: Y-13836470-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.13836470G>A , CM000686.2:g.13836470G>A GRCh38
NC_000024.9:g.15948350G>A , CM000686.1:g.15948350G>A GRCh37
NC_000024.8:g.14457744G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000652544.1:n.685-22047G>A
ENST00000430079.5:n.478-17974G>A
ENST00000460561.1:n.261-22047G>A
ENST00000472227.5:n.399-22032G>A
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