Canonical Allele Identifier: CA342143482

Gene: HJV

Linked Data

• ClinVar Variation Id: 2041931
• ClinVar RCV Id: RCV002903354
• dbSNP Id: rs1195704136
• gnomAD v2: 1-145415378-G-A
• gnomAD v3: 1-146019635-C-T
• gnomAD v4: 1-146019635-C-T
• MyVariant Identifiers: chr1:g.145415378G>A (hg19) ; chr1:g.146019635C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.146019635C>T , CM000663.2:g.146019635C>T	GRCh38
NC_000001.10:g.145415378G>A , CM000663.1:g.145415378G>A	GRCh37
NC_000001.9:g.144126735G>A	NCBI36
NG_011568.1:g.7188G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336751.11:c.197G>A MANE Select	ENSP00000337014.5:p.Gly66Glu
ENST00000636675.1:c.-22+63G>A	ENSP00000490072.1:n.-22+63G>A
ENST00000336751.10:c.197G>A	ENSP00000337014.5:p.Gly66Glu
ENST00000357836.5:c.-143G>A	ENSP00000350495.5:n.-143G>A
ENST00000421822.2:c.197G>A	ENSP00000411863.2:p.Gly66Glu
ENST00000475797.1:c.-21-935G>A	ENSP00000425716.1:n.-21-935G>A
ENST00000497365.5:c.-22+63G>A	ENSP00000421820.1:n.-22+63G>A
ENST00000634927.1:c.134+63G>A	ENSP00000489347.1:n.134+63G>A
NM_001316767.1:c.-22+63G>A	NP_001303696.1:n.-22+63G>A
NM_145277.4:c.-143G>A	NP_660320.3:n.-143G>A
NM_202004.3:c.-22+63G>A	NP_973733.1:n.-22+63G>A
NM_213652.3:c.-21-935G>A	NP_998817.1:n.-21-935G>A
NM_213653.3:c.197G>A	NP_998818.1:p.Gly66Glu
XM_005272932.1:c.197G>A	XP_005272989.1:p.Gly66Glu
NM_001316767.2:c.-22+63G>A	NP_001303696.1:n.-22+63G>A
NM_145277.5:c.-143G>A	NP_660320.3:n.-143G>A
NM_202004.4:c.-22+63G>A	NP_973733.1:n.-22+63G>A
NM_213652.4:c.-21-935G>A	NP_998817.1:n.-21-935G>A
NM_001379352.1:c.197G>A	NP_001366281.1:p.Gly66Glu
NM_213653.4:c.197G>A MANE Select	NP_998818.1:p.Gly66Glu