HGVS | Genome Assembly |
---|---|
NC_000005.10:g.38482183A>G , CM000667.2:g.38482183A>G | GRCh38 |
NC_000005.9:g.38482285A>G , CM000667.1:g.38482285A>G | GRCh37 |
NC_000005.8:g.38518042A>G | NCBI36 |
NG_011817.1:g.118223T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000453190.7:c.2706T>C MANE Select | ENSP00000398368.2:p.Pro902= | |
ENST00000263409.8:c.2706T>C | ENSP00000263409.4:p.Pro902= | |
ENST00000453190.6:c.2706T>C | ENSP00000398368.2:p.Pro902= | |
NM_001127671.1:c.2706T>C | NP_001121143.1:p.Pro902= | |
NM_002310.5:c.2706T>C | NP_002301.1:p.Pro902= | |
XM_011514040.1:c.2706T>C | XP_011512342.1:p.Pro902= | |
XM_011514041.1:c.2706T>C | XP_011512343.1:p.Pro902= | |
XM_011514042.1:c.2706T>C | XP_011512344.1:p.Pro902= | |
NM_001364297.1:c.2706T>C | NP_001351226.1:p.Pro902= | |
NM_001364298.1:c.2673T>C | NP_001351227.1:p.Pro891= | |
XM_011514042.3:c.2706T>C | XP_011512344.1:p.Pro902= | |
XM_017009462.1:c.2760T>C | XP_016864951.1:p.Pro920= | |
XM_017009463.1:c.2706T>C | XP_016864952.1:p.Pro902= | |
NM_001127671.2:c.2706T>C MANE Select | NP_001121143.1:p.Pro902= | |
NM_002310.6:c.2706T>C | NP_002301.1:p.Pro902= | |
NM_001364297.2:c.2706T>C | NP_001351226.1:p.Pro902= | |
NM_001364298.2:c.2673T>C | NP_001351227.1:p.Pro891= |