Canonical Allele Identifier: CA352494729

Gene: PTH1R

Linked Data

• gnomAD v4: 3-46897959-C-G
• MyVariant Identifiers: chr3:g.46939449C>G (hg19) ; chr3:g.46897959C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46897959C>G , CM000665.2:g.46897959C>G	GRCh38
NC_000003.11:g.46939449C>G , CM000665.1:g.46939449C>G	GRCh37
NC_000003.10:g.46914453C>G	NCBI36
NG_008864.1:g.25214C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449590.6:c.418C>G MANE Select	ENSP00000402723.1:p.His140Asp
ENST00000313049.9:c.418C>G	ENSP00000321999.4:p.His140Asp
ENST00000418619.5:c.418C>G	ENSP00000411424.1:p.His140Asp
ENST00000427125.6:c.418C>G	ENSP00000400977.2:p.His140Asp
ENST00000428220.1:c.418C>G	ENSP00000389811.1:p.His140Asp
ENST00000430002.6:c.418C>G	ENSP00000413774.2:p.His140Asp
ENST00000449590.5:c.418C>G	ENSP00000402723.1:p.His140Asp
ENST00000490109.1:n.438C>G
NM_000316.2:c.418C>G	NP_000307.1:p.His140Asp
NM_001184744.1:c.418C>G	NP_001171673.1:p.His140Asp
XM_005265344.2:c.325C>G	XP_005265401.1:p.His109Asp
XM_011533967.1:c.457C>G	XP_011532269.1:p.His153Asp
XM_011533968.1:c.439C>G	XP_011532270.1:p.His147Asp
XM_005265344.3:c.325C>G	XP_005265401.1:p.His109Asp
XM_011533967.3:c.457C>G	XP_011532269.1:p.His153Asp
XM_011533968.2:c.439C>G	XP_011532270.1:p.His147Asp
XM_017006932.2:c.457C>G	XP_016862421.1:p.His153Asp
XM_017006933.1:c.418C>G	XP_016862422.1:p.His140Asp
XM_017006934.1:c.457C>G	XP_016862423.1:p.His153Asp
NM_000316.3:c.418C>G MANE Select	NP_000307.1:p.His140Asp