HGVS | Genome Assembly |
---|---|
NC_000008.11:g.64604828A>G , CM000670.2:g.64604828A>G | GRCh38 |
NC_000008.10:g.65517385A>G , CM000670.1:g.65517385A>G | GRCh37 |
NC_000008.9:g.65679939A>G | NCBI36 |
NG_008338.1:g.198964T>C | |
NG_008338.2:g.198964T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000310193.4:c.1087T>C MANE Select | ENSP00000310721.3:p.Ser363Pro | |
ENST00000310193.3:c.1087T>C | ENSP00000310721.3:p.Ser363Pro | |
ENST00000523954.1:n.361T>C | ||
NM_004820.3:c.1087T>C | NP_004811.1:p.Ser363Pro | |
NM_001324112.1:c.1087T>C | NP_001311041.1:p.Ser363Pro | |
NM_004820.4:c.1087T>C | NP_004811.1:p.Ser363Pro | |
XM_017014002.1:c.1153T>C | XP_016869491.1:p.Ser385Pro | |
NM_004820.5:c.1087T>C MANE Select | NP_004811.1:p.Ser363Pro | |
NM_001324112.2:c.1087T>C | NP_001311041.1:p.Ser363Pro |