Canonical Allele Identifier: CA337511148

Gene: RPS4Y2

Linked Data

• dbSNP Id: rs1043501101
• MyVariant Identifiers: chrY:g.22921697T>C (hg19) ; chrY:g.20759811T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.20759811T>C , CM000686.2:g.20759811T>C	GRCh38
NC_000024.9:g.22921697T>C , CM000686.1:g.22921697T>C	GRCh37
NC_000024.8:g.21331085T>C	NCBI36
NG_032924.1:g.8744T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000629237.2:c.82-57T>C MANE Select	ENSP00000486252.1:n.82-57T>C
ENST00000629237.1:c.82-57T>C	ENSP00000486252.1:n.82-57T>C
NM_001039567.2:c.82-57T>C	NP_001034656.1:n.82-57T>C
XM_011531423.1:c.31-57T>C	XP_011529725.1:n.31-57T>C
NM_001039567.3:c.82-57T>C MANE Select	NP_001034656.1:n.82-57T>C