Canonical Allele Identifier: CA645235416
Gene: RPS4Y2 HGNC NCBI

Linked Data

dbSNP Id: rs753162642
gnomAD v2: Y-22918046-C-T
MyVariant Identifiers: chrY:g.22918046C>T (hg19) chrY:g.20756160C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20756160C>T , CM000686.2:g.20756160C>T GRCh38
NC_000024.9:g.22918046C>T , CM000686.1:g.22918046C>T GRCh37
NC_000024.8:g.21327434C>T NCBI36
NG_032924.1:g.5093C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000629237.2:c.-4C>T MANE Select ENSP00000486252.1:n.-4C>T
NM_001039567.2:c.-4C>T NP_001034656.1:n.-4C>T
NM_001039567.3:c.-4C>T MANE Select NP_001034656.1:n.-4C>T
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