Canonical Allele Identifier: CA414858238
Gene: RPS4Y2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.22921778C>A (hg19) chrY:g.20759892C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20759892C>A , CM000686.2:g.20759892C>A GRCh38
NC_000024.9:g.22921778C>A , CM000686.1:g.22921778C>A GRCh37
NC_000024.8:g.21331166C>A NCBI36
NG_032924.1:g.8825C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000629237.2:c.106C>A MANE Select ENSP00000486252.1:p.His36Asn
ENST00000629237.1:c.106C>A ENSP00000486252.1:p.His36Asn
NM_001039567.2:c.106C>A NP_001034656.1:p.His36Asn
XM_011531423.1:c.55C>A XP_011529725.1:p.His19Asn
NM_001039567.3:c.106C>A MANE Select NP_001034656.1:p.His36Asn
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