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Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.1505410G= , CM000678.2:g.1505410G=
GRCh38
NC_000016.9:g.1555411G= , CM000678.1:g.1555411G=
GRCh37
NC_000016.8:g.1495412G=
NCBI36
NG_050910.1:g.17067G=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000262319.11:c.1843G=
MANE Select
ENSP00000262319.6:p.Val615=
ENST00000262319.10:c.1843G=
ENSP00000262319.6:p.Val615=
ENST00000497339.6:c.1228-863G=
ENSP00000456383.1:n.1228-863G=
ENST00000564507.5:n.438G=
ENST00000567423.1:c.263G=
ENST00000567427.1:n.42G=
ENST00000569744.1:n.272G=
NM_016111.3:c.1843G=
NP_057195.2:p.Val615=
XM_006720993.2:c.1843G=
XP_006721056.1:p.Val615=
XM_011522773.1:c.1843G=
XP_011521075.1:p.Val615=
XM_011522774.1:c.1843G=
XP_011521076.1:p.Val615=
XM_011522775.1:c.1843G=
XP_011521077.1:p.Val615=
XM_011522776.1:c.1843G=
XP_011521078.1:p.Val615=
XM_011522777.1:c.1843G=
XP_011521079.1:p.Val615=
XM_011522778.1:c.1843G=
XP_011521080.1:p.Val615=
XR_932982.1:n.2129G=
XR_932983.1:n.2049G=
NM_001351846.1:c.1843G=
NP_001338775.1:p.Val615=
XM_011522773.3:c.1843G=
XP_011521075.1:p.Val615=
XM_011522774.2:c.1843G=
XP_011521076.1:p.Val615=
XM_011522775.3:c.1843G=
XP_011521077.1:p.Val615=
XM_011522776.2:c.1843G=
XP_011521078.1:p.Val615=
XM_011522777.3:c.1843G=
XP_011521079.1:p.Val615=
XM_011522778.3:c.1843G=
XP_011521080.1:p.Val615=
XR_001752042.2:n.1907G=
XR_001752043.2:n.1890G=
XR_001752044.2:n.1827G=
XR_932982.3:n.1907G=
NM_016111.4:c.1843G=
MANE Select
NP_057195.2:p.Val615=
NM_001351846.2:c.1843G=
NP_001338775.1:p.Val615=