Canonical Allele Identifier: CA414858503

Gene: RPS4Y2

Linked Data

• MyVariant Identifiers: chrY:g.22921848A>C (hg19) ; chrY:g.20759962A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.20759962A>C , CM000686.2:g.20759962A>C	GRCh38
NC_000024.9:g.22921848A>C , CM000686.1:g.22921848A>C	GRCh37
NC_000024.8:g.21331236A>C	NCBI36
NG_032924.1:g.8895A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000629237.2:c.176A>C MANE Select	ENSP00000486252.1:p.Asp59Ala
ENST00000629237.1:c.176A>C	ENSP00000486252.1:p.Asp59Ala
NM_001039567.2:c.176A>C	NP_001034656.1:p.Asp59Ala
XM_011531423.1:c.125A>C	XP_011529725.1:p.Asp42Ala
NM_001039567.3:c.176A>C MANE Select	NP_001034656.1:p.Asp59Ala