Canonical Allele Identifier: CA414858220

Gene: RPS4Y2

Linked Data

• COSMIC: COSM5699998
• MyVariant Identifiers: chrY:g.22921773G>A (hg19) ; chrY:g.20759887G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.20759887G>A , CM000686.2:g.20759887G>A	GRCh38
NC_000024.9:g.22921773G>A , CM000686.1:g.22921773G>A	GRCh37
NC_000024.8:g.21331161G>A	NCBI36
NG_032924.1:g.8820G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000629237.2:c.101G>A MANE Select	ENSP00000486252.1:p.Gly34Asp
ENST00000629237.1:c.101G>A	ENSP00000486252.1:p.Gly34Asp
NM_001039567.2:c.101G>A	NP_001034656.1:p.Gly34Asp
XM_011531423.1:c.50G>A	XP_011529725.1:p.Gly17Asp
NM_001039567.3:c.101G>A MANE Select	NP_001034656.1:p.Gly34Asp