Canonical Allele Identifier: CA414858499

Gene: RPS4Y2

Linked Data

• MyVariant Identifiers: chrY:g.22921847G>T (hg19) ; chrY:g.20759961G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.20759961G>T , CM000686.2:g.20759961G>T	GRCh38
NC_000024.9:g.22921847G>T , CM000686.1:g.22921847G>T	GRCh37
NC_000024.8:g.21331235G>T	NCBI36
NG_032924.1:g.8894G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000629237.2:c.175G>T MANE Select	ENSP00000486252.1:p.Asp59Tyr
ENST00000629237.1:c.175G>T	ENSP00000486252.1:p.Asp59Tyr
NM_001039567.2:c.175G>T	NP_001034656.1:p.Asp59Tyr
XM_011531423.1:c.124G>T	XP_011529725.1:p.Asp42Tyr
NM_001039567.3:c.175G>T MANE Select	NP_001034656.1:p.Asp59Tyr