Canonical Allele Identifier: CA1139656289

Gene: HJV

Linked Data

• ClinVar Variation Id: 875017
• ClinVar RCV Id: RCV001098478
• dbSNP Id: rs1652426841
• gnomAD v4: 1-146017880-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.146017880C>T , CM000663.2:g.146017880C>T	GRCh38
NC_000001.10:g.145417133G>A , CM000663.1:g.145417133G>A	GRCh37
NC_000001.9:g.144128490G>A	NCBI36
NG_011568.1:g.8943G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336751.11:c.*197G>A MANE Select	ENSP00000337014.5:n.*197G>A
ENST00000636675.1:c.*197G>A	ENSP00000490072.1:n.*197G>A
ENST00000336751.10:c.*197G>A	ENSP00000337014.5:n.*197G>A
ENST00000357836.5:c.*197G>A	ENSP00000350495.5:n.*197G>A
ENST00000475797.1:c.*197G>A	ENSP00000425716.1:n.*197G>A
ENST00000497365.5:c.*197G>A	ENSP00000421820.1:n.*197G>A
NM_001316767.1:c.*197G>A	NP_001303696.1:n.*197G>A
NM_145277.4:c.*197G>A	NP_660320.3:n.*197G>A
NM_202004.3:c.*197G>A	NP_973733.1:n.*197G>A
NM_213652.3:c.*197G>A	NP_998817.1:n.*197G>A
NM_213653.3:c.*197G>A	NP_998818.1:n.*197G>A
XM_005272932.1:c.*197G>A	XP_005272989.1:n.*197G>A
NM_001316767.2:c.*197G>A	NP_001303696.1:n.*197G>A
NM_145277.5:c.*197G>A	NP_660320.3:n.*197G>A
NM_202004.4:c.*197G>A	NP_973733.1:n.*197G>A
NM_213652.4:c.*197G>A	NP_998817.1:n.*197G>A
NM_001379352.1:c.*197G>A	NP_001366281.1:n.*197G>A
NM_213653.4:c.*197G>A MANE Select	NP_998818.1:n.*197G>A