Canonical Allele Identifier: CA342135258
Gene: HJV HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.146018413C>A , CM000663.2:g.146018413C>A GRCh38
NC_000001.10:g.145416600G>T , CM000663.1:g.145416600G>T GRCh37
NC_000001.9:g.144127957G>T NCBI36
NG_011568.1:g.8410G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000336751.11:c.945G>T MANE Select ENSP00000337014.5:p.Gln315His
ENST00000636675.1:c.267G>T ENSP00000490072.1:p.Gln89His
ENST00000336751.10:c.945G>T ENSP00000337014.5:p.Gln315His
ENST00000357836.5:c.606G>T ENSP00000350495.5:p.Gln202His
ENST00000475797.1:c.267G>T ENSP00000425716.1:p.Gln89His
ENST00000497365.5:c.267G>T ENSP00000421820.1:p.Gln89His
NM_001316767.1:c.267G>T NP_001303696.1:p.Gln89His
NM_145277.4:c.606G>T NP_660320.3:p.Gln202His
NM_202004.3:c.267G>T NP_973733.1:p.Gln89His
NM_213652.3:c.267G>T NP_998817.1:p.Gln89His
NM_213653.3:c.945G>T NP_998818.1:p.Gln315His
XM_005272932.1:c.945G>T XP_005272989.1:p.Gln315His
NM_001316767.2:c.267G>T NP_001303696.1:p.Gln89His
NM_145277.5:c.606G>T NP_660320.3:p.Gln202His
NM_202004.4:c.267G>T NP_973733.1:p.Gln89His
NM_213652.4:c.267G>T NP_998817.1:p.Gln89His
NM_001379352.1:c.945G>T NP_001366281.1:p.Gln315His
NM_213653.4:c.945G>T MANE Select NP_998818.1:p.Gln315His