Canonical Allele Identifier: CA1139347751
Gene: ANOS2P HGNC NCBI

Linked Data

dbSNP Id: rs2079820374
gnomAD v3: Y-13836266-T-C
gnomAD v4: Y-13836266-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.13836266T>C , CM000686.2:g.13836266T>C GRCh38
NC_000024.9:g.15948146T>C , CM000686.1:g.15948146T>C GRCh37
NC_000024.8:g.14457540T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000652544.1:n.685-22251T>C
ENST00000430079.5:n.478-18178T>C
ENST00000460561.1:n.261-22251T>C
ENST00000472227.5:n.399-22236T>C