Canonical Allele Identifier: CA327517329
Gene: PHEX HGNC NCBI

Linked Data

dbSNP Id: rs921596276
gnomAD v4: X-22032903-T-G
MyVariant Identifiers: chrX:g.22051021T>G (hg19) chrX:g.22032903T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22032903T>G , CM000685.2:g.22032903T>G GRCh38
NC_000023.10:g.22051021T>G , CM000685.1:g.22051021T>G GRCh37
NC_000023.9:g.21960942T>G NCBI36
NG_007563.2:g.5101T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000475778.2:n.324T>G
ENST00000683214.1:n.324T>G
ENST00000684143.1:c.-103T>G ENSP00000508264.1:n.-103T>G
ENST00000379374.5:c.-103T>G MANE Select ENSP00000368682.4:n.-103T>G
ENST00000379374.4:c.-103T>G ENSP00000368682.4:n.-103T>G
NM_000444.5:c.-103T>G NP_000435.3:n.-103T>G
NM_001282754.1:c.-103T>G NP_001269683.1:n.-103T>G
XM_011545535.1:c.-103T>G XP_011543837.1:n.-103T>G
XR_001755695.1:n.577T>G
NM_000444.6:c.-103T>G MANE Select NP_000435.3:n.-103T>G
NM_001282754.2:c.-103T>G NP_001269683.1:n.-103T>G
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