Canonical Allele Identifier: CA414857764
Gene: RPS4Y2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.22918677A>C (hg19) chrY:g.20756791A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20756791A>C , CM000686.2:g.20756791A>C GRCh38
NC_000024.9:g.22918677A>C , CM000686.1:g.22918677A>C GRCh37
NC_000024.8:g.21328065A>C NCBI36
NG_032924.1:g.5724A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000629237.2:c.17A>C MANE Select ENSP00000486252.1:p.Lys6Thr
ENST00000629237.1:c.17A>C ENSP00000486252.1:p.Lys6Thr
NM_001039567.2:c.17A>C NP_001034656.1:p.Lys6Thr
NM_001039567.3:c.17A>C MANE Select NP_001034656.1:p.Lys6Thr
Search 100 bp 5'
Search 100 bp 3'