HGVS | Genome Assembly |
---|---|
NC_000014.9:g.36663189C= , CM000676.2:g.36663189C= | GRCh38 |
NC_000014.8:g.37132394C= , CM000676.1:g.37132394C= | GRCh37 |
NC_000014.7:g.36202145C= | NCBI36 |
NG_013357.1:g.10622C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361487.7:c.297C= MANE Select | ENSP00000355245.6:p.Ala99= | |
ENST00000361487.6:c.297C= | ENSP00000355245.6:p.Ala99= | |
ENST00000402703.6:c.297C= | ENSP00000384817.2:p.Ala99= | |
ENST00000554201.1:c.-265C= | ENSP00000450434.1:n.-265C= | |
NM_006194.3:c.297C= | NP_006185.1:p.Ala99= | |
NM_001372076.1:c.297C= MANE Select | NP_001359005.1:p.Ala99= | |
NM_006194.4:c.297C= | NP_006185.1:p.Ala99= |