Canonical Allele Identifier: CA473263537

Gene: PTH

Linked Data

• gnomAD v4: 11-13492585-A-T
• MyVariant Identifiers: chr11:g.13514132A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.13492585A>T , CM000673.2:g.13492585A>T	GRCh38
NC_000011.9:g.13514132A>T , CM000673.1:g.13514132A>T	GRCh37
NC_000011.8:g.13470708A>T	NCBI36
NG_008962.1:g.8436T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282091.6:c.168T>A MANE Select	ENSP00000282091.1:p.Arg56=
ENST00000282091.5:c.168T>A	ENSP00000282091.1:p.Arg56=
ENST00000529816.1:c.168T>A	ENSP00000433208.1:p.Arg56=
NM_000315.2:c.168T>A	NP_000306.1:p.Arg56=
NM_000315.3:c.168T>A	NP_000306.1:p.Arg56=
NM_001316352.1:c.264T>A	NP_001303281.1:p.Arg88=
NM_000315.4:c.168T>A MANE Select	NP_000306.1:p.Arg56=
NM_001316352.2:c.264T>A	NP_001303281.1:p.Arg88=