Canonical Allele Identifier: CA1139342315
Gene: ANOS2P HGNC NCBI

Linked Data

dbSNP Id: rs2079799820
gnomAD v3: Y-13787188-A-G
gnomAD v4: Y-13787188-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.13787188A>G , CM000686.2:g.13787188A>G GRCh38
NC_000024.9:g.15899068A>G , CM000686.1:g.15899068A>G GRCh37
NC_000024.8:g.14408462A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000652544.1:n.684+32399A>G
ENST00000430079.5:n.430-3731A>G
ENST00000460561.1:n.213-3731A>G
ENST00000472227.5:n.351-3731A>G