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Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.34489338C= , CM000671.2:g.34489338C=
GRCh38
NC_000009.11:g.34489336C= , CM000671.1:g.34489336C=
GRCh37
NC_000009.10:g.34479336C=
NCBI36
NG_008127.1:g.35526C=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000242317.9:c.277C=
MANE Select
ENSP00000242317.4:p.Pro93=
ENST00000242317.8:c.277C=
ENSP00000242317.4:p.Pro93=
ENST00000437363.5:c.244C=
ENSP00000395396.1:p.Pro82=
ENST00000488369.1:n.393C=
ENST00000614641.4:c.277C=
ENSP00000480538.1:p.Pro93=
NM_001281428.1:c.277C=
NP_001268357.1:p.Pro93=
NM_012144.3:c.277C=
NP_036276.1:p.Pro93=
XM_011517846.1:c.277C=
XP_011516148.1:p.Pro93=
XM_011517847.1:c.277C=
XP_011516149.1:p.Pro93=
XM_011517848.1:c.277C=
XP_011516150.1:p.Pro93=
XM_011517849.1:c.277C=
XP_011516151.1:p.Pro93=
XM_011517850.1:c.277C=
XP_011516152.1:p.Pro93=
XR_929232.1:n.531C=
XR_929233.1:n.531C=
XR_929235.1:n.531C=
XM_006716758.3:c.-200C=
XP_006716821.1:n.-200C=
XM_011517846.2:c.277C=
XP_011516148.1:p.Pro93=
XM_011517847.3:c.277C=
XP_011516149.1:p.Pro93=
XM_011517848.2:c.277C=
XP_011516150.1:p.Pro93=
XM_011517849.2:c.277C=
XP_011516151.1:p.Pro93=
XM_011517850.3:c.277C=
XP_011516152.1:p.Pro93=
XM_017014625.2:c.277C=
XP_016870114.1:p.Pro93=
XR_002956774.1:n.478C=
XR_929232.2:n.478C=
XR_929233.2:n.478C=
NM_012144.4:c.277C=
MANE Select
NP_036276.1:p.Pro93=
NM_001281428.2:c.277C=
NP_001268357.1:p.Pro93=