Canonical Allele Identifier: CA414858327

Gene: RPS4Y2

Linked Data

• MyVariant Identifiers: chrY:g.22921802C>A (hg19) ; chrY:g.20759916C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.20759916C>A , CM000686.2:g.20759916C>A	GRCh38
NC_000024.9:g.22921802C>A , CM000686.1:g.22921802C>A	GRCh37
NC_000024.8:g.21331190C>A	NCBI36
NG_032924.1:g.8849C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000629237.2:c.130C>A MANE Select	ENSP00000486252.1:p.Leu44Met
ENST00000629237.1:c.130C>A	ENSP00000486252.1:p.Leu44Met
NM_001039567.2:c.130C>A	NP_001034656.1:p.Leu44Met
XM_011531423.1:c.79C>A	XP_011529725.1:p.Leu27Met
NM_001039567.3:c.130C>A MANE Select	NP_001034656.1:p.Leu44Met