Canonical Allele Identifier: CA414947382
Gene: RPS4Y1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.2734869G>C (hg19) chrY:g.2866828G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2866828G>C , CM000686.2:g.2866828G>C GRCh38
NC_000024.9:g.2734869G>C , CM000686.1:g.2734869G>C GRCh37
NC_000024.8:g.2794869G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000250784.13:c.726G>C MANE Select ENSP00000250784.7:p.Lys242Asn
ENST00000250784.12:c.726G>C ENSP00000250784.7:p.Lys242Asn
ENST00000430575.1:c.753G>C ENSP00000415317.1:p.Lys251Asn
ENST00000477725.1:n.870G>C
ENST00000515575.1:n.42+12057G>C
NM_001008.3:c.726G>C NP_000999.1:p.Lys242Asn
NM_001008.4:c.726G>C MANE Select NP_000999.1:p.Lys242Asn
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