Canonical Allele Identifier: CA414857758
Gene: RPS4Y2 HGNC NCBI

Linked Data

COSMIC: COSM4157077
MyVariant Identifiers: chrY:g.22918674C>G (hg19) chrY:g.20756788C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20756788C>G , CM000686.2:g.20756788C>G GRCh38
NC_000024.9:g.22918674C>G , CM000686.1:g.22918674C>G GRCh37
NC_000024.8:g.21328062C>G NCBI36
NG_032924.1:g.5721C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000629237.2:c.14C>G MANE Select ENSP00000486252.1:p.Pro5Arg
ENST00000629237.1:c.14C>G ENSP00000486252.1:p.Pro5Arg
NM_001039567.2:c.14C>G NP_001034656.1:p.Pro5Arg
NM_001039567.3:c.14C>G MANE Select NP_001034656.1:p.Pro5Arg
Search 100 bp 5'
Search 100 bp 3'