Canonical Allele Identifier: CA1198821003

Gene: HJV

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.146018539A= , CM000663.2:g.146018539A=	GRCh38
NC_000001.10:g.145416474T= , CM000663.1:g.145416474T=	GRCh37
NC_000001.9:g.144127831T=	NCBI36
NG_011568.1:g.8284T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336751.11:c.819T= MANE Select	ENSP00000337014.5:p.His273=
ENST00000636675.1:c.141T=	ENSP00000490072.1:p.His47=
ENST00000336751.10:c.819T=	ENSP00000337014.5:p.His273=
ENST00000357836.5:c.480T=	ENSP00000350495.5:p.His160=
ENST00000475797.1:c.141T=	ENSP00000425716.1:p.His47=
ENST00000497365.5:c.141T=	ENSP00000421820.1:p.His47=
NM_001316767.1:c.141T=	NP_001303696.1:p.His47=
NM_145277.4:c.480T=	NP_660320.3:p.His160=
NM_202004.3:c.141T=	NP_973733.1:p.His47=
NM_213652.3:c.141T=	NP_998817.1:p.His47=
NM_213653.3:c.819T=	NP_998818.1:p.His273=
XM_005272932.1:c.819T=	XP_005272989.1:p.His273=
NM_001316767.2:c.141T=	NP_001303696.1:p.His47=
NM_145277.5:c.480T=	NP_660320.3:p.His160=
NM_202004.4:c.141T=	NP_973733.1:p.His47=
NM_213652.4:c.141T=	NP_998817.1:p.His47=
NM_001379352.1:c.819T=	NP_001366281.1:p.His273=
NM_213653.4:c.819T= MANE Select	NP_998818.1:p.His273=