Canonical Allele Identifier: CA880352344
Gene: RPS4Y1 HGNC NCBI

Linked Data

dbSNP Id: rs1393731438
MyVariant Identifiers: chrY:g.2722488G>A (hg19) chrY:g.2854447G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2854447G>A , CM000686.2:g.2854447G>A GRCh38
NC_000024.9:g.2722488G>A , CM000686.1:g.2722488G>A GRCh37
NC_000024.8:g.2782488G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000681940.1:n.205-153G>A
ENST00000250784.13:c.361-153G>A MANE Select ENSP00000250784.7:n.361-153G>A
ENST00000250784.12:c.361-153G>A ENSP00000250784.7:n.361-153G>A
ENST00000430575.1:c.388-153G>A ENSP00000415317.1:n.388-153G>A
ENST00000477725.1:n.352G>A
NM_001008.3:c.361-153G>A NP_000999.1:n.361-153G>A
NM_001008.4:c.361-153G>A MANE Select NP_000999.1:n.361-153G>A
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