HGVS | Genome Assembly |
---|---|
NC_000001.11:g.186679430A>T , CM000663.2:g.186679430A>T | GRCh38 |
NC_000001.10:g.186648562A>T , CM000663.1:g.186648562A>T | GRCh37 |
NC_000001.9:g.184915185A>T | NCBI36 |
NG_028206.2:g.5998T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367468.10:c.61T>A MANE Select | ENSP00000356438.5:p.Cys21Ser | |
ENST00000680451.1:c.61T>A | ENSP00000506242.1:p.Cys21Ser | |
ENST00000681605.1:c.61T>A | ENSP00000504900.1:p.Cys21Ser | |
ENST00000367468.9:c.61T>A | ENSP00000356438.5:p.Cys21Ser | |
ENST00000490885.6:n.194T>A | ||
ENST00000559627.1:c.61T>A | ENSP00000454130.1:p.Cys21Ser | |
ENST00000559800.1:n.194T>A | ||
NM_000963.3:c.61T>A | NP_000954.1:p.Cys21Ser | |
NM_000963.4:c.61T>A MANE Select | NP_000954.1:p.Cys21Ser |