Canonical Allele Identifier: CA2605369729
Gene: HHIP HGNC NCBI

Linked Data

dbSNP Id: rs2126683256

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144728833A>G , CM000666.2:g.144728833A>G GRCh38
NC_000004.11:g.145649985A>G , CM000666.1:g.145649985A>G GRCh37
NC_000004.10:g.145869435A>G NCBI36
NG_011496.1:g.87813A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000296575.8:c.1761-5908A>G MANE Select ENSP00000296575.3:n.1761-5908A>G
ENST00000649263.1:c.328-312855T>C ENSP00000497507.1:n.328-312855T>C
ENST00000296575.7:c.1761-5908A>G ENSP00000296575.3:n.1761-5908A>G
NM_022475.2:c.1761-5908A>G NP_071920.1:n.1761-5908A>G
XM_005263178.3:c.1761-5908A>G XP_005263235.1:n.1761-5908A>G
XM_006714288.2:c.1761-5908A>G XP_006714351.1:n.1761-5908A>G
XM_005263178.5:c.1761-5908A>G XP_005263235.1:n.1761-5908A>G
XM_006714288.4:c.1761-5908A>G XP_006714351.1:n.1761-5908A>G
NM_022475.3:c.1761-5908A>G MANE Select NP_071920.1:n.1761-5908A>G