Canonical Allele Identifier: CA1500800374
Gene: HHIP HGNC NCBI

Linked Data

dbSNP Id: rs1730868917
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144728827G>A , CM000666.2:g.144728827G>A GRCh38
NC_000004.11:g.145649979G>A , CM000666.1:g.145649979G>A GRCh37
NC_000004.10:g.145869429G>A NCBI36
NG_011496.1:g.87807G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000296575.8:c.1761-5914G>A MANE Select ENSP00000296575.3:n.1761-5914G>A
ENST00000649263.1:c.328-312849C>T ENSP00000497507.1:n.328-312849C>T
ENST00000296575.7:c.1761-5914G>A ENSP00000296575.3:n.1761-5914G>A
NM_022475.2:c.1761-5914G>A NP_071920.1:n.1761-5914G>A
XM_005263178.3:c.1761-5914G>A XP_005263235.1:n.1761-5914G>A
XM_006714288.2:c.1761-5914G>A XP_006714351.1:n.1761-5914G>A
XM_005263178.5:c.1761-5914G>A XP_005263235.1:n.1761-5914G>A
XM_006714288.4:c.1761-5914G>A XP_006714351.1:n.1761-5914G>A
NM_022475.3:c.1761-5914G>A MANE Select NP_071920.1:n.1761-5914G>A
Search 100 bp 5'
Search 100 bp 3'