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Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.154448154G= , CM000663.2:g.154448154G=
GRCh38
NC_000001.10:g.154420630G= , CM000663.1:g.154420630G=
GRCh37
NC_000001.9:g.152687254G=
NCBI36
NG_012087.1:g.47962G=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000368485.8:c.979G=
MANE Select
ENSP00000357470.3:p.Val327=
ENST00000344086.8:c.979G=
ENSP00000340589.4:p.Val327=
ENST00000368485.7:c.979G=
ENSP00000357470.3:p.Val327=
ENST00000476006.5:c.795G=
ENST00000507256.1:n.177G=
ENST00000515190.1:c.387G=
NM_000565.3:c.979G=
NP_000556.1:p.Val327=
NM_181359.2:c.979G=
NP_852004.1:p.Val327=
XM_005245139.1:c.837G=
XP_005245196.1:p.Arg279=
XM_005245140.1:c.837G=
XP_005245197.1:p.Arg279=
XM_006711298.1:c.1027G=
XP_006711361.1:p.Val343=
XM_006711299.2:c.1027G=
XP_006711362.1:p.Val343=
XM_005245139.2:c.837G=
XP_005245196.1:p.Arg279=
XM_005245140.3:c.837G=
XP_005245197.1:p.Arg279=
XM_006711298.2:c.1027G=
XP_006711361.1:p.Val343=
XM_006711299.4:c.1027G=
XP_006711362.1:p.Val343=
XM_017001199.2:c.1027G=
XP_016856688.1:p.Val343=
XM_017001200.2:c.979G=
XP_016856689.1:p.Val327=
XM_017001201.2:c.837G=
XP_016856690.1:p.Arg279=
NM_000565.4:c.979G=
MANE Select
NP_000556.1:p.Val327=
NM_181359.3:c.979G=
NP_852004.1:p.Val327=
NM_001382769.1:c.979G=
NP_001369698.1:p.Val327=
NM_001382770.1:c.1072G=
NP_001369699.1:p.Val358=
NM_001382771.1:c.1027G=
NP_001369700.1:p.Val343=
NM_001382772.1:c.973G=
NP_001369701.1:p.Val325=
NM_001382773.1:c.1027G=
NP_001369702.1:p.Val343=
NM_001382774.1:c.619G=
NP_001369703.1:p.Val207=