Canonical Allele Identifier: CA473263490

Gene: PTH

Linked Data

• MyVariant Identifiers: chr11:g.13514066A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.13492519A>T , CM000673.2:g.13492519A>T	GRCh38
NC_000011.9:g.13514066A>T , CM000673.1:g.13514066A>T	GRCh37
NC_000011.8:g.13470642A>T	NCBI36
NG_008962.1:g.8502T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282091.6:c.234T>A MANE Select	ENSP00000282091.1:p.Gly78=
ENST00000282091.5:c.234T>A	ENSP00000282091.1:p.Gly78=
ENST00000529816.1:c.234T>A	ENSP00000433208.1:p.Gly78=
NM_000315.2:c.234T>A	NP_000306.1:p.Gly78=
NM_000315.3:c.234T>A	NP_000306.1:p.Gly78=
NM_001316352.1:c.330T>A	NP_001303281.1:p.Gly110=
NM_000315.4:c.234T>A MANE Select	NP_000306.1:p.Gly78=
NM_001316352.2:c.330T>A	NP_001303281.1:p.Gly110=