Canonical Allele Identifier: CA1053984

Gene: HJV

Linked Data

• ClinVar Variation Id: 1084752
• ClinVar RCV Id: RCV001401861
• dbSNP Id: rs782705517
• ExAC: 1:145416882 C / T
• gnomAD v2: 1-145416882-C-T
• gnomAD v4: 1-146018131-G-A
• MyVariant Identifiers: chr1:g.145416882C>T (hg19) ; chr1:g.146018131G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.146018131G>A , CM000663.2:g.146018131G>A	GRCh38
NC_000001.10:g.145416882C>T , CM000663.1:g.145416882C>T	GRCh37
NC_000001.9:g.144128239C>T	NCBI36
NG_011568.1:g.8692C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336751.11:c.1227C>T MANE Select	ENSP00000337014.5:p.Thr409=
ENST00000636675.1:c.549C>T	ENSP00000490072.1:p.Thr183=
ENST00000336751.10:c.1227C>T	ENSP00000337014.5:p.Thr409=
ENST00000357836.5:c.888C>T	ENSP00000350495.5:p.Thr296=
ENST00000475797.1:c.549C>T	ENSP00000425716.1:p.Thr183=
ENST00000497365.5:c.549C>T	ENSP00000421820.1:p.Thr183=
NM_001316767.1:c.549C>T	NP_001303696.1:p.Thr183=
NM_145277.4:c.888C>T	NP_660320.3:p.Thr296=
NM_202004.3:c.549C>T	NP_973733.1:p.Thr183=
NM_213652.3:c.549C>T	NP_998817.1:p.Thr183=
NM_213653.3:c.1227C>T	NP_998818.1:p.Thr409=
XM_005272932.1:c.1227C>T	XP_005272989.1:p.Thr409=
NM_001316767.2:c.549C>T	NP_001303696.1:p.Thr183=
NM_145277.5:c.888C>T	NP_660320.3:p.Thr296=
NM_202004.4:c.549C>T	NP_973733.1:p.Thr183=
NM_213652.4:c.549C>T	NP_998817.1:p.Thr183=
NM_001379352.1:c.1227C>T	NP_001366281.1:p.Thr409=
NM_213653.4:c.1227C>T MANE Select	NP_998818.1:p.Thr409=