Canonical Allele Identifier: CA520176572
Gene: RPS4Y2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.22921855A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20759969A>T , CM000686.2:g.20759969A>T GRCh38
NC_000024.9:g.22921855A>T , CM000686.1:g.22921855A>T GRCh37
NC_000024.8:g.21331243A>T NCBI36
NG_032924.1:g.8902A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000629237.2:c.183A>T MANE Select ENSP00000486252.1:p.Val61=
ENST00000629237.1:c.183A>T ENSP00000486252.1:p.Val61=
NM_001039567.2:c.183A>T NP_001034656.1:p.Val61=
XM_011531423.1:c.132A>T XP_011529725.1:p.Val44=
NM_001039567.3:c.183A>T MANE Select NP_001034656.1:p.Val61=