Canonical Allele Identifier: CA1620106170
Gene: ITPR3 HGNC NCBI

Linked Data

dbSNP Id: rs1240001886

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33650328G>T , CM000668.2:g.33650328G>T GRCh38
NC_000006.11:g.33618105G>T , CM000668.1:g.33618105G>T GRCh37
NC_000006.10:g.33726083G>T NCBI36
NG_027729.1:g.33950G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000605930.3:c.161-5438G>T MANE Select ENSP00000475177.1:n.161-5438G>T
ENST00000374316.9:c.161-5438G>T ENSP00000363435.4:n.161-5438G>T
ENST00000605930.2:c.161-5438G>T ENSP00000475177.1:n.161-5438G>T
NM_002224.3:c.161-5438G>T NP_002215.2:n.161-5438G>T
XM_011514576.1:c.230-5438G>T XP_011512878.1:n.230-5438G>T
XM_017010832.1:c.161-5438G>T XP_016866321.1:n.161-5438G>T
NM_002224.4:c.161-5438G>T MANE Select NP_002215.2:n.161-5438G>T