Canonical Allele Identifier: CA1041777643

Gene: PTH2R

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208713876T>C , CM000664.2:g.208713876T>C	GRCh38
NC_000002.11:g.209578600T>C , CM000664.1:g.209578600T>C	GRCh37
NC_000002.10:g.209286845T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419079.1:c.426+56887T>C
XR_241394.2:n.469+56887T>C
XR_923817.1:n.469+56887T>C
XR_923818.1:n.469+56887T>C
XR_923819.1:n.469+56887T>C
XR_923820.1:n.469+56887T>C
XR_923821.1:n.469+56887T>C
XR_923822.1:n.469+56887T>C
XR_923823.1:n.469+56887T>C
XR_923824.1:n.469+56887T>C
XR_923825.1:n.469+56887T>C
XR_923826.1:n.469+56887T>C
XR_923827.1:n.469+56887T>C
XR_923828.1:n.469+56887T>C
XR_923829.1:n.469+56887T>C
XR_923830.1:n.622+56887T>C
XR_923831.1:n.686+56887T>C
XR_923832.1:n.469+56887T>C
XR_923833.1:n.338+56887T>C
XR_923834.1:n.469+56887T>C
XR_923835.1:n.469+56887T>C
XR_923836.1:n.469+56887T>C
XR_923837.1:n.3005+56887T>C
XR_923838.1:n.239+56887T>C
NR_136588.1:n.669+56887T>C