HGVS | Genome Assembly |
---|---|
NC_000011.10:g.116832878T>C , CM000673.2:g.116832878T>C | GRCh38 |
NC_000011.9:g.116703594T>C , CM000673.1:g.116703594T>C | GRCh37 |
NC_000011.8:g.116208804T>C | NCBI36 |
NG_008949.1:g.7971T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000227667.8:c.294T>C MANE Select | ENSP00000227667.2:p.Ala98= | |
ENST00000227667.7:c.294T>C | ENSP00000227667.2:p.Ala98= | |
ENST00000375345.3:c.348T>C | ENSP00000364494.1:p.Ala116= | |
ENST00000630701.1:c.348T>C | ENSP00000486182.1:p.Ala116= | |
NM_000040.1:c.294T>C | NP_000031.1:p.Ala98= | |
NM_000040.2:c.294T>C | NP_000031.1:p.Ala98= | |
NM_000040.3:c.294T>C MANE Select | NP_000031.1:p.Ala98= |