Canonical Allele Identifier: CA788470207
Gene: HHIP HGNC NCBI

Linked Data

dbSNP Id: rs1402633731
gnomAD v3: 4-144728896-G-A
gnomAD v4: 4-144728896-G-A
MyVariant Identifiers: chr4:g.145650048G>A (hg19) chr4:g.144728896G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144728896G>A , CM000666.2:g.144728896G>A GRCh38
NC_000004.11:g.145650048G>A , CM000666.1:g.145650048G>A GRCh37
NC_000004.10:g.145869498G>A NCBI36
NG_011496.1:g.87876G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000296575.8:c.1761-5845G>A MANE Select ENSP00000296575.3:n.1761-5845G>A
ENST00000649263.1:c.328-312918C>T ENSP00000497507.1:n.328-312918C>T
ENST00000296575.7:c.1761-5845G>A ENSP00000296575.3:n.1761-5845G>A
NM_022475.2:c.1761-5845G>A NP_071920.1:n.1761-5845G>A
XM_005263178.3:c.1761-5845G>A XP_005263235.1:n.1761-5845G>A
XM_006714288.2:c.1761-5845G>A XP_006714351.1:n.1761-5845G>A
XM_005263178.5:c.1761-5845G>A XP_005263235.1:n.1761-5845G>A
XM_006714288.4:c.1761-5845G>A XP_006714351.1:n.1761-5845G>A
NM_022475.3:c.1761-5845G>A MANE Select NP_071920.1:n.1761-5845G>A
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