Canonical Allele Identifier: CA337639409
Gene: RBMY3AP HGNC NCBI

Linked Data

dbSNP Id: rs35567891
gnomAD v3: Y-9610745-A-G
gnomAD v4: Y-9610745-A-G
MyVariant Identifiers: chrY:g.9448354A>G (hg19) chrY:g.9610745A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.9610745A>G , CM000686.2:g.9610745A>G GRCh38
NC_000024.9:g.9448354A>G , CM000686.1:g.9448354A>G GRCh37
NC_000024.8:g.10058354A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000449381.1:n.971T>C
NR_001573.1:n.293T>C
NR_001573.2:n.293T>C
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