Canonical Allele Identifier: CA414858662

Gene: RPS4Y2

Linked Data

• MyVariant Identifiers: chrY:g.22921881T>A (hg19) ; chrY:g.20759995T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.20759995T>A , CM000686.2:g.20759995T>A	GRCh38
NC_000024.9:g.22921881T>A , CM000686.1:g.22921881T>A	GRCh37
NC_000024.8:g.21331269T>A	NCBI36
NG_032924.1:g.8928T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000629237.2:c.209T>A MANE Select	ENSP00000486252.1:p.Leu70His
ENST00000629237.1:c.209T>A	ENSP00000486252.1:p.Leu70His
NM_001039567.2:c.209T>A	NP_001034656.1:p.Leu70His
XM_011531423.1:c.158T>A	XP_011529725.1:p.Leu53His
NM_001039567.3:c.209T>A MANE Select	NP_001034656.1:p.Leu70His