Canonical Allele Identifier: CA515423856
Gene: PHEX HGNC NCBI

Linked Data

ClinVar Variation Id: 1113494
ClinVar RCV Id: RCV001440900
dbSNP Id: rs1456105345
gnomAD v2: X-22051195-C-T
gnomAD v3: X-22033077-C-T
gnomAD v4: X-22033077-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.22033077C>T , CM000685.2:g.22033077C>T GRCh38
NC_000023.10:g.22051195C>T , CM000685.1:g.22051195C>T GRCh37
NC_000023.9:g.21961116C>T NCBI36
NG_007563.2:g.5275C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000475778.2:n.498C>T
ENST00000683214.1:n.498C>T
ENST00000684143.1:c.72C>T ENSP00000508264.1:p.Val24=
ENST00000379374.5:c.72C>T MANE Select ENSP00000368682.4:p.Val24=
ENST00000379374.4:c.72C>T ENSP00000368682.4:p.Val24=
NM_000444.5:c.72C>T NP_000435.3:p.Val24=
NM_001282754.1:c.72C>T NP_001269683.1:p.Val24=
XM_011545535.1:c.72C>T XP_011543837.1:p.Val24=
XR_001755695.1:n.751C>T
NM_000444.6:c.72C>T MANE Select NP_000435.3:p.Val24=
NM_001282754.2:c.72C>T NP_001269683.1:p.Val24=