Canonical Allele Identifier: CA420250221

Gene: HJV

Linked Data

• MyVariant Identifiers: chr1:g.145416750T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.146018263A>C , CM000663.2:g.146018263A>C	GRCh38
NC_000001.10:g.145416750T>G , CM000663.1:g.145416750T>G	GRCh37
NC_000001.9:g.144128107T>G	NCBI36
NG_011568.1:g.8560T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336751.11:c.1095T>G MANE Select	ENSP00000337014.5:p.Val365=
ENST00000636675.1:c.417T>G	ENSP00000490072.1:p.Val139=
ENST00000336751.10:c.1095T>G	ENSP00000337014.5:p.Val365=
ENST00000357836.5:c.756T>G	ENSP00000350495.5:p.Val252=
ENST00000475797.1:c.417T>G	ENSP00000425716.1:p.Val139=
ENST00000497365.5:c.417T>G	ENSP00000421820.1:p.Val139=
NM_001316767.1:c.417T>G	NP_001303696.1:p.Val139=
NM_145277.4:c.756T>G	NP_660320.3:p.Val252=
NM_202004.3:c.417T>G	NP_973733.1:p.Val139=
NM_213652.3:c.417T>G	NP_998817.1:p.Val139=
NM_213653.3:c.1095T>G	NP_998818.1:p.Val365=
XM_005272932.1:c.1095T>G	XP_005272989.1:p.Val365=
NM_001316767.2:c.417T>G	NP_001303696.1:p.Val139=
NM_145277.5:c.756T>G	NP_660320.3:p.Val252=
NM_202004.4:c.417T>G	NP_973733.1:p.Val139=
NM_213652.4:c.417T>G	NP_998817.1:p.Val139=
NM_001379352.1:c.1095T>G	NP_001366281.1:p.Val365=
NM_213653.4:c.1095T>G MANE Select	NP_998818.1:p.Val365=