HGVS | Genome Assembly |
---|---|
NC_000014.9:g.36663124G>A , CM000676.2:g.36663124G>A | GRCh38 |
NC_000014.8:g.37132329G>A , CM000676.1:g.37132329G>A | GRCh37 |
NC_000014.7:g.36202080G>A | NCBI36 |
NG_013357.1:g.10557G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361487.7:c.232G>A MANE Select | ENSP00000355245.6:p.Val78Ile | |
ENST00000555639.2:c.232G>A | ENSP00000501203.1:p.Val78Ile | |
ENST00000361487.6:c.232G>A | ENSP00000355245.6:p.Val78Ile | |
ENST00000402703.6:c.232G>A | ENSP00000384817.2:p.Val78Ile | |
ENST00000554201.1:c.-330G>A | ENSP00000450434.1:n.-330G>A | |
ENST00000555639.1:n.534G>A | ||
NM_006194.3:c.232G>A | NP_006185.1:p.Val78Ile | |
NM_001372076.1:c.232G>A MANE Select | NP_001359005.1:p.Val78Ile | |
NM_006194.4:c.232G>A | NP_006185.1:p.Val78Ile |