Canonical Allele Identifier: CA520175339
Gene: RPS4Y2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.22918669G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20756783G>T , CM000686.2:g.20756783G>T GRCh38
NC_000024.9:g.22918669G>T , CM000686.1:g.22918669G>T GRCh37
NC_000024.8:g.21328057G>T NCBI36
NG_032924.1:g.5716G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000629237.2:c.9G>T MANE Select ENSP00000486252.1:p.Arg3=
ENST00000629237.1:c.9G>T ENSP00000486252.1:p.Arg3=
NM_001039567.2:c.9G>T NP_001034656.1:p.Arg3=
NM_001039567.3:c.9G>T MANE Select NP_001034656.1:p.Arg3=
Search 100 bp 5'
Search 100 bp 3'