HGVS | Genome Assembly |
---|---|
NC_000007.14:g.17339488C>A , CM000669.2:g.17339488C>A | GRCh38 |
NC_000007.13:g.17379112C>A , CM000669.1:g.17379112C>A | GRCh37 |
NC_000007.12:g.17345637C>A | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000242057.9:c.1663C>A MANE Select | ENSP00000242057.4:p.His555Asn | |
ENST00000637807.1:c.1633C>A | ENSP00000490530.1:p.His545Asn | |
ENST00000642825.1:c.1618C>A | ENSP00000495987.1:p.His540Asn | |
ENST00000242057.8:c.1663C>A | ENSP00000242057.4:p.His555Asn | |
ENST00000463496.1:c.1663C>A | ENSP00000436466.1:p.His555Asn | |
ENST00000492120.1:n.645C>A | ||
NM_001621.4:c.1663C>A | NP_001612.1:p.His555Asn | |
NM_001621.5:c.1663C>A MANE Select | NP_001612.1:p.His555Asn |