Canonical Allele Identifier: CA379724502
Gene: PTH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.13492493T>A , CM000673.2:g.13492493T>A GRCh38
NC_000011.9:g.13514040T>A , CM000673.1:g.13514040T>A GRCh37
NC_000011.8:g.13470616T>A NCBI36
NG_008962.1:g.8528A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000282091.6:c.260A>T MANE Select ENSP00000282091.1:p.Asp87Val
ENST00000282091.5:c.260A>T ENSP00000282091.1:p.Asp87Val
ENST00000529816.1:c.260A>T ENSP00000433208.1:p.Asp87Val
NM_000315.2:c.260A>T NP_000306.1:p.Asp87Val
NM_000315.3:c.260A>T NP_000306.1:p.Asp87Val
NM_001316352.1:c.356A>T NP_001303281.1:p.Asp119Val
NM_000315.4:c.260A>T MANE Select NP_000306.1:p.Asp87Val
NM_001316352.2:c.356A>T NP_001303281.1:p.Asp119Val