Canonical Allele Identifier: CA414857752
Gene: RPS4Y2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.22918671G>C (hg19) chrY:g.20756785G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20756785G>C , CM000686.2:g.20756785G>C GRCh38
NC_000024.9:g.22918671G>C , CM000686.1:g.22918671G>C GRCh37
NC_000024.8:g.21328059G>C NCBI36
NG_032924.1:g.5718G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000629237.2:c.11G>C MANE Select ENSP00000486252.1:p.Gly4Ala
ENST00000629237.1:c.11G>C ENSP00000486252.1:p.Gly4Ala
NM_001039567.2:c.11G>C NP_001034656.1:p.Gly4Ala
NM_001039567.3:c.11G>C MANE Select NP_001034656.1:p.Gly4Ala
Search 100 bp 5'
Search 100 bp 3'