Canonical Allele Identifier: CA29822901

Gene: HJV

Linked Data

• ClinVar Variation Id: 752678
• ClinVar RCV Id: RCV000929838
• dbSNP Id: rs782552789
• gnomAD v3: 1-146018164-G-C
• gnomAD v4: 1-146018164-G-C
• MyVariant Identifiers: chr1:g.145416849C>G (hg19) ; chr1:g.146018164G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.146018164G>C , CM000663.2:g.146018164G>C	GRCh38
NC_000001.10:g.145416849C>G , CM000663.1:g.145416849C>G	GRCh37
NC_000001.9:g.144128206C>G	NCBI36
NG_011568.1:g.8659C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336751.11:c.1194C>G MANE Select	ENSP00000337014.5:p.Pro398=
ENST00000636675.1:c.516C>G	ENSP00000490072.1:p.Pro172=
ENST00000336751.10:c.1194C>G	ENSP00000337014.5:p.Pro398=
ENST00000357836.5:c.855C>G	ENSP00000350495.5:p.Pro285=
ENST00000475797.1:c.516C>G	ENSP00000425716.1:p.Pro172=
ENST00000497365.5:c.516C>G	ENSP00000421820.1:p.Pro172=
NM_001316767.1:c.516C>G	NP_001303696.1:p.Pro172=
NM_145277.4:c.855C>G	NP_660320.3:p.Pro285=
NM_202004.3:c.516C>G	NP_973733.1:p.Pro172=
NM_213652.3:c.516C>G	NP_998817.1:p.Pro172=
NM_213653.3:c.1194C>G	NP_998818.1:p.Pro398=
XM_005272932.1:c.1194C>G	XP_005272989.1:p.Pro398=
NM_001316767.2:c.516C>G	NP_001303696.1:p.Pro172=
NM_145277.5:c.855C>G	NP_660320.3:p.Pro285=
NM_202004.4:c.516C>G	NP_973733.1:p.Pro172=
NM_213652.4:c.516C>G	NP_998817.1:p.Pro172=
NM_001379352.1:c.1194C>G	NP_001366281.1:p.Pro398=
NM_213653.4:c.1194C>G MANE Select	NP_998818.1:p.Pro398=