Canonical Allele Identifier: CA337511820
Gene: RPS4Y2 HGNC NCBI

Linked Data

dbSNP Id: rs1039583403
MyVariant Identifiers: chrY:g.22940576G>C (hg19) chrY:g.20778690G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20778690G>C , CM000686.2:g.20778690G>C GRCh38
NC_000024.9:g.22940576G>C , CM000686.1:g.22940576G>C GRCh37
NC_000024.8:g.21349964G>C NCBI36
NG_032924.1:g.27623G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000629237.2:c.533-819G>C MANE Select ENSP00000486252.1:n.533-819G>C
ENST00000629237.1:c.533-819G>C ENSP00000486252.1:n.533-819G>C
NM_001039567.2:c.533-819G>C NP_001034656.1:n.533-819G>C
XM_011531423.1:c.482-819G>C XP_011529725.1:n.482-819G>C
NM_001039567.3:c.533-819G>C MANE Select NP_001034656.1:n.533-819G>C
Search 100 bp 5'
Search 100 bp 3'