Canonical Allele Identifier: CA1053811

Gene: HJV

Linked Data

• ClinVar Variation Id: 1535439
• ClinVar RCV Id: RCV002072675
• dbSNP Id: rs782020534
• ExAC: 1:145415592 C / G
• gnomAD v2: 1-145415592-C-G
• gnomAD v3: 1-146019421-G-C
• gnomAD v4: 1-146019421-G-C
• MyVariant Identifiers: chr1:g.145415592C>G (hg19) ; chr1:g.146019421G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.146019421G>C , CM000663.2:g.146019421G>C	GRCh38
NC_000001.10:g.145415592C>G , CM000663.1:g.145415592C>G	GRCh37
NC_000001.9:g.144126949C>G	NCBI36
NG_011568.1:g.7402C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336751.11:c.411C>G MANE Select	ENSP00000337014.5:p.Gly137=
ENST00000636675.1:c.-22+277C>G	ENSP00000490072.1:n.-22+277C>G
ENST00000336751.10:c.411C>G	ENSP00000337014.5:p.Gly137=
ENST00000357836.5:c.72C>G	ENSP00000350495.5:p.Gly24=
ENST00000475797.1:c.-21-721C>G	ENSP00000425716.1:n.-21-721C>G
ENST00000497365.5:c.-22+277C>G	ENSP00000421820.1:n.-22+277C>G
ENST00000634927.1:c.134+277C>G	ENSP00000489347.1:n.134+277C>G
NM_001316767.1:c.-22+277C>G	NP_001303696.1:n.-22+277C>G
NM_145277.4:c.72C>G	NP_660320.3:p.Gly24=
NM_202004.3:c.-22+277C>G	NP_973733.1:n.-22+277C>G
NM_213652.3:c.-21-721C>G	NP_998817.1:n.-21-721C>G
NM_213653.3:c.411C>G	NP_998818.1:p.Gly137=
XM_005272932.1:c.411C>G	XP_005272989.1:p.Gly137=
NM_001316767.2:c.-22+277C>G	NP_001303696.1:n.-22+277C>G
NM_145277.5:c.72C>G	NP_660320.3:p.Gly24=
NM_202004.4:c.-22+277C>G	NP_973733.1:n.-22+277C>G
NM_213652.4:c.-21-721C>G	NP_998817.1:n.-21-721C>G
NM_001379352.1:c.411C>G	NP_001366281.1:p.Gly137=
NM_213653.4:c.411C>G MANE Select	NP_998818.1:p.Gly137=