Canonical Allele Identifier: CA788470138
Gene: HHIP HGNC NCBI

Linked Data

dbSNP Id: rs1361994173
MyVariant Identifiers: chr4:g.145649939G>C (hg19) chr4:g.144728787G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144728787G>C , CM000666.2:g.144728787G>C GRCh38
NC_000004.11:g.145649939G>C , CM000666.1:g.145649939G>C GRCh37
NC_000004.10:g.145869389G>C NCBI36
NG_011496.1:g.87767G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000296575.8:c.1761-5954G>C MANE Select ENSP00000296575.3:n.1761-5954G>C
ENST00000649263.1:c.328-312809C>G ENSP00000497507.1:n.328-312809C>G
ENST00000296575.7:c.1761-5954G>C ENSP00000296575.3:n.1761-5954G>C
NM_022475.2:c.1761-5954G>C NP_071920.1:n.1761-5954G>C
XM_005263178.3:c.1761-5954G>C XP_005263235.1:n.1761-5954G>C
XM_006714288.2:c.1761-5954G>C XP_006714351.1:n.1761-5954G>C
XM_005263178.5:c.1761-5954G>C XP_005263235.1:n.1761-5954G>C
XM_006714288.4:c.1761-5954G>C XP_006714351.1:n.1761-5954G>C
NM_022475.3:c.1761-5954G>C MANE Select NP_071920.1:n.1761-5954G>C
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