Canonical Allele Identifier: CA337737954

Gene: ANOS2P

Linked Data

• dbSNP Id: rs10436792
• gnomAD v3: Y-13765774-T-C
• gnomAD v4: Y-13765774-T-C
• MyVariant Identifiers: chrY:g.15877654T>C (hg19) ; chrY:g.13765774T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.13765774T>C , CM000686.2:g.13765774T>C	GRCh38
NC_000024.9:g.15877654T>C , CM000686.1:g.15877654T>C	GRCh37
NC_000024.8:g.14387048T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000652544.1:n.684+10985T>C
ENST00000430079.5:n.429+10985T>C
ENST00000460561.1:n.212+10985T>C
ENST00000472227.5:n.350+13769T>C