Canonical Allele Identifier: CA1053758
Gene: HJV HGNC NCBI

Linked Data

dbSNP Id: rs782488465

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.146019668C>A , CM000663.2:g.146019668C>A GRCh38
NC_000001.10:g.145415345G>T , CM000663.1:g.145415345G>T GRCh37
NC_000001.9:g.144126702G>T NCBI36
NG_011568.1:g.7155G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000336751.11:c.164G>T MANE Select ENSP00000337014.5:p.Gly55Val
ENST00000636675.1:c.-22+30G>T ENSP00000490072.1:n.-22+30G>T
ENST00000336751.10:c.164G>T ENSP00000337014.5:p.Gly55Val
ENST00000357836.5:c.-176G>T ENSP00000350495.5:n.-176G>T
ENST00000421822.2:c.164G>T ENSP00000411863.2:p.Gly55Val
ENST00000475797.1:c.-21-968G>T ENSP00000425716.1:n.-21-968G>T
ENST00000497365.5:c.-22+30G>T ENSP00000421820.1:n.-22+30G>T
ENST00000634927.1:c.134+30G>T ENSP00000489347.1:n.134+30G>T
NM_001316767.1:c.-22+30G>T NP_001303696.1:n.-22+30G>T
NM_145277.4:c.-176G>T NP_660320.3:n.-176G>T
NM_202004.3:c.-22+30G>T NP_973733.1:n.-22+30G>T
NM_213652.3:c.-21-968G>T NP_998817.1:n.-21-968G>T
NM_213653.3:c.164G>T NP_998818.1:p.Gly55Val
XM_005272932.1:c.164G>T XP_005272989.1:p.Gly55Val
NM_001316767.2:c.-22+30G>T NP_001303696.1:n.-22+30G>T
NM_145277.5:c.-176G>T NP_660320.3:n.-176G>T
NM_202004.4:c.-22+30G>T NP_973733.1:n.-22+30G>T
NM_213652.4:c.-21-968G>T NP_998817.1:n.-21-968G>T
NM_001379352.1:c.164G>T NP_001366281.1:p.Gly55Val
NM_213653.4:c.164G>T MANE Select NP_998818.1:p.Gly55Val