Canonical Allele Identifier: CA352496321

Gene: PTH1R

Linked Data

• dbSNP Id: rs1257887202
• gnomAD v2: 3-46940190-T-G
• MyVariant Identifiers: chr3:g.46940190T>G (hg19) ; chr3:g.46898700T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46898700T>G , CM000665.2:g.46898700T>G	GRCh38
NC_000003.11:g.46940190T>G , CM000665.1:g.46940190T>G	GRCh37
NC_000003.10:g.46915194T>G	NCBI36
NG_008864.1:g.25955T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000449590.6:c.677T>G MANE Select	ENSP00000402723.1:p.Leu226Arg
ENST00000313049.9:c.677T>G	ENSP00000321999.4:p.Leu226Arg
ENST00000418619.5:c.677T>G	ENSP00000411424.1:p.Leu226Arg
ENST00000427125.6:c.677T>G	ENSP00000400977.2:p.Leu226Arg
ENST00000428220.1:c.677T>G	ENSP00000389811.1:p.Leu226Arg
ENST00000430002.6:c.677T>G	ENSP00000413774.2:p.Leu226Arg
ENST00000449590.5:c.677T>G	ENSP00000402723.1:p.Leu226Arg
ENST00000490109.1:n.697T>G
NM_000316.2:c.677T>G	NP_000307.1:p.Leu226Arg
NM_001184744.1:c.677T>G	NP_001171673.1:p.Leu226Arg
XM_005265344.2:c.584T>G	XP_005265401.1:p.Leu195Arg
XM_011533967.1:c.716T>G	XP_011532269.1:p.Leu239Arg
XM_011533968.1:c.698T>G	XP_011532270.1:p.Leu233Arg
XM_005265344.3:c.584T>G	XP_005265401.1:p.Leu195Arg
XM_011533967.3:c.716T>G	XP_011532269.1:p.Leu239Arg
XM_011533968.2:c.698T>G	XP_011532270.1:p.Leu233Arg
XM_017006932.2:c.716T>G	XP_016862421.1:p.Leu239Arg
XM_017006933.1:c.677T>G	XP_016862422.1:p.Leu226Arg
XM_017006934.1:c.716T>G	XP_016862423.1:p.Leu239Arg
NM_000316.3:c.677T>G MANE Select	NP_000307.1:p.Leu226Arg