HGVS | Genome Assembly |
---|---|
NC_000009.12:g.38395908T>C , CM000671.2:g.38395908T>C | GRCh38 |
NC_000009.11:g.38395905T>C , CM000671.1:g.38395905T>C | GRCh37 |
NC_000009.10:g.38385905T>C | NCBI36 |
NG_012253.1:g.8204T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000377698.4:c.160T>C MANE Select | ENSP00000366927.3:p.Phe54Leu | |
ENST00000377698.3:c.160T>C | ENSP00000366927.3:p.Phe54Leu | |
ENST00000635162.1:c.160T>C | ENSP00000489053.1:p.Phe54Leu | |
NM_000692.4:c.160T>C | NP_000683.3:p.Phe54Leu | |
XM_011517802.1:c.160T>C | XP_011516104.1:p.Phe54Leu | |
XM_011517802.2:c.160T>C | XP_011516104.1:p.Phe54Leu | |
NM_000692.5:c.160T>C MANE Select | NP_000683.3:p.Phe54Leu |