Canonical Allele Identifier: CA1198821066

Gene: HJV

Linked Data

• ClinVar Variation Id: 1547468
• ClinVar RCV Id: RCV002173448
• dbSNP Id: rs1652508396

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.146018707G>A , CM000663.2:g.146018707G>A	GRCh38
NC_000001.10:g.145416306C>T , CM000663.1:g.145416306C>T	GRCh37
NC_000001.9:g.144127663C>T	NCBI36
NG_011568.1:g.8116C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000336751.11:c.658-7C>T MANE Select	ENSP00000337014.5:n.658-7C>T
ENST00000636675.1:c.-21-7C>T	ENSP00000490072.1:n.-21-7C>T
ENST00000336751.10:c.658-7C>T	ENSP00000337014.5:n.658-7C>T
ENST00000357836.5:c.319-7C>T	ENSP00000350495.5:n.319-7C>T
ENST00000475797.1:c.-21-7C>T	ENSP00000425716.1:n.-21-7C>T
ENST00000497365.5:c.-21-7C>T	ENSP00000421820.1:n.-21-7C>T
ENST00000634927.1:c.135-7C>T	ENSP00000489347.1:n.135-7C>T
NM_001316767.1:c.-21-7C>T	NP_001303696.1:n.-21-7C>T
NM_145277.4:c.319-7C>T	NP_660320.3:n.319-7C>T
NM_202004.3:c.-21-7C>T	NP_973733.1:n.-21-7C>T
NM_213652.3:c.-21-7C>T	NP_998817.1:n.-21-7C>T
NM_213653.3:c.658-7C>T	NP_998818.1:n.658-7C>T
XM_005272932.1:c.658-7C>T	XP_005272989.1:n.658-7C>T
NM_001316767.2:c.-21-7C>T	NP_001303696.1:n.-21-7C>T
NM_145277.5:c.319-7C>T	NP_660320.3:n.319-7C>T
NM_202004.4:c.-21-7C>T	NP_973733.1:n.-21-7C>T
NM_213652.4:c.-21-7C>T	NP_998817.1:n.-21-7C>T
NM_001379352.1:c.658-7C>T	NP_001366281.1:n.658-7C>T
NM_213653.4:c.658-7C>T MANE Select	NP_998818.1:n.658-7C>T