Canonical Allele Identifier: CA342134488

Gene: HJV

Linked Data

• ClinVar Variation Id: 1511768
• ClinVar RCV Id: RCV002020581
• dbSNP Id: rs1652462514
• gnomAD v3: 1-146018336-T-A
• gnomAD v4: 1-146018336-T-A
• MyVariant Identifiers: chr1:g.145416677A>T (hg19) ; chr1:g.146018336T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.146018336T>A , CM000663.2:g.146018336T>A	GRCh38
NC_000001.10:g.145416677A>T , CM000663.1:g.145416677A>T	GRCh37
NC_000001.9:g.144128034A>T	NCBI36
NG_011568.1:g.8487A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000336751.11:c.1022A>T MANE Select	ENSP00000337014.5:p.Asp341Val
ENST00000636675.1:c.344A>T	ENSP00000490072.1:p.Asp115Val
ENST00000336751.10:c.1022A>T	ENSP00000337014.5:p.Asp341Val
ENST00000357836.5:c.683A>T	ENSP00000350495.5:p.Asp228Val
ENST00000475797.1:c.344A>T	ENSP00000425716.1:p.Asp115Val
ENST00000497365.5:c.344A>T	ENSP00000421820.1:p.Asp115Val
NM_001316767.1:c.344A>T	NP_001303696.1:p.Asp115Val
NM_145277.4:c.683A>T	NP_660320.3:p.Asp228Val
NM_202004.3:c.344A>T	NP_973733.1:p.Asp115Val
NM_213652.3:c.344A>T	NP_998817.1:p.Asp115Val
NM_213653.3:c.1022A>T	NP_998818.1:p.Asp341Val
XM_005272932.1:c.1022A>T	XP_005272989.1:p.Asp341Val
NM_001316767.2:c.344A>T	NP_001303696.1:p.Asp115Val
NM_145277.5:c.683A>T	NP_660320.3:p.Asp228Val
NM_202004.4:c.344A>T	NP_973733.1:p.Asp115Val
NM_213652.4:c.344A>T	NP_998817.1:p.Asp115Val
NM_001379352.1:c.1022A>T	NP_001366281.1:p.Asp341Val
NM_213653.4:c.1022A>T MANE Select	NP_998818.1:p.Asp341Val