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Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.73978072C= , CM000673.2:g.73978072C=
GRCh38
NC_000011.9:g.73689117C= , CM000673.1:g.73689117C=
GRCh37
NC_000011.8:g.73366765C=
NCBI36
NG_011478.1:g.9773G=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000310473.9:c.151G=
ENSP00000312029.3:p.Val51=
ENST00000663595.2:c.151G=
MANE Select
ENSP00000499695.1:p.Val51=
ENST00000310473.7:c.151G=
ENSP00000312029.3:p.Val51=
ENST00000536983.5:c.151G=
ENSP00000441147.1:p.Val51=
ENST00000544615.5:c.70G=
ENSP00000439951.1:p.Val24=
NM_003355.2:c.151G=
NP_003346.2:p.Val51=
XM_024448674.1:c.154G=
XP_024304442.1:p.Val52=
NM_001381943.1:c.151G=
NP_001368872.1:p.Val51=
NM_001381944.1:c.151G=
NP_001368873.1:p.Val51=
NM_001381945.1:c.151G=
NP_001368874.1:p.Val51=
NM_001381947.1:c.151G=
NP_001368876.1:p.Val51=
NM_001381948.1:c.151G=
NP_001368877.1:p.Val51=
NM_001381949.1:c.151G=
NP_001368878.1:p.Val51=
NM_001381950.1:c.151G=
NP_001368879.1:p.Val51=
NM_003355.3:c.151G=
MANE Select
NP_003346.2:p.Val51=