Canonical Allele Identifier: CA107720978

Gene: HHIP

Linked Data

• dbSNP Id: rs1032619977
• MyVariant Identifiers: chr4:g.145649878T>C (hg19) ; chr4:g.144728726T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.144728726T>C , CM000666.2:g.144728726T>C	GRCh38
NC_000004.11:g.145649878T>C , CM000666.1:g.145649878T>C	GRCh37
NC_000004.10:g.145869328T>C	NCBI36
NG_011496.1:g.87706T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296575.8:c.1761-6015T>C MANE Select	ENSP00000296575.3:n.1761-6015T>C
ENST00000649263.1:c.328-312748A>G	ENSP00000497507.1:n.328-312748A>G
ENST00000296575.7:c.1761-6015T>C	ENSP00000296575.3:n.1761-6015T>C
NM_022475.2:c.1761-6015T>C	NP_071920.1:n.1761-6015T>C
XM_005263178.3:c.1761-6015T>C	XP_005263235.1:n.1761-6015T>C
XM_006714288.2:c.1761-6015T>C	XP_006714351.1:n.1761-6015T>C
XM_005263178.5:c.1761-6015T>C	XP_005263235.1:n.1761-6015T>C
XM_006714288.4:c.1761-6015T>C	XP_006714351.1:n.1761-6015T>C
NM_022475.3:c.1761-6015T>C MANE Select	NP_071920.1:n.1761-6015T>C