Canonical Allele Identifier: CA420603383
Gene: HJV HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.145416612G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.146018401C>A , CM000663.2:g.146018401C>A GRCh38
NC_000001.10:g.145416612G>T , CM000663.1:g.145416612G>T GRCh37
NC_000001.9:g.144127969G>T NCBI36
NG_011568.1:g.8422G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000336751.11:c.957G>T MANE Select ENSP00000337014.5:p.Gly319=
ENST00000636675.1:c.279G>T ENSP00000490072.1:p.Gly93=
ENST00000336751.10:c.957G>T ENSP00000337014.5:p.Gly319=
ENST00000357836.5:c.618G>T ENSP00000350495.5:p.Gly206=
ENST00000475797.1:c.279G>T ENSP00000425716.1:p.Gly93=
ENST00000497365.5:c.279G>T ENSP00000421820.1:p.Gly93=
NM_001316767.1:c.279G>T NP_001303696.1:p.Gly93=
NM_145277.4:c.618G>T NP_660320.3:p.Gly206=
NM_202004.3:c.279G>T NP_973733.1:p.Gly93=
NM_213652.3:c.279G>T NP_998817.1:p.Gly93=
NM_213653.3:c.957G>T NP_998818.1:p.Gly319=
XM_005272932.1:c.957G>T XP_005272989.1:p.Gly319=
NM_001316767.2:c.279G>T NP_001303696.1:p.Gly93=
NM_145277.5:c.618G>T NP_660320.3:p.Gly206=
NM_202004.4:c.279G>T NP_973733.1:p.Gly93=
NM_213652.4:c.279G>T NP_998817.1:p.Gly93=
NM_001379352.1:c.957G>T NP_001366281.1:p.Gly319=
NM_213653.4:c.957G>T MANE Select NP_998818.1:p.Gly319=