Canonical Allele Identifier: CA414857774
Gene: RPS4Y2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.22918679A>C (hg19) chrY:g.20756793A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20756793A>C , CM000686.2:g.20756793A>C GRCh38
NC_000024.9:g.22918679A>C , CM000686.1:g.22918679A>C GRCh37
NC_000024.8:g.21328067A>C NCBI36
NG_032924.1:g.5726A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000629237.2:c.19A>C MANE Select ENSP00000486252.1:p.Lys7Gln
ENST00000629237.1:c.19A>C ENSP00000486252.1:p.Lys7Gln
NM_001039567.2:c.19A>C NP_001034656.1:p.Lys7Gln
XM_011531423.1:c.-202A>C XP_011529725.1:n.-202A>C
NM_001039567.3:c.19A>C MANE Select NP_001034656.1:p.Lys7Gln
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