Canonical Allele Identifier: CA414857761
Gene: RPS4Y2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.22918676A>T (hg19) chrY:g.20756790A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20756790A>T , CM000686.2:g.20756790A>T GRCh38
NC_000024.9:g.22918676A>T , CM000686.1:g.22918676A>T GRCh37
NC_000024.8:g.21328064A>T NCBI36
NG_032924.1:g.5723A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000629237.2:c.16A>T MANE Select ENSP00000486252.1:p.Lys6Ter
ENST00000629237.1:c.16A>T ENSP00000486252.1:p.Lys6Ter
NM_001039567.2:c.16A>T NP_001034656.1:p.Lys6Ter
NM_001039567.3:c.16A>T MANE Select NP_001034656.1:p.Lys6Ter
Search 100 bp 5'
Search 100 bp 3'