HGVS | Genome Assembly |
---|---|
NC_000007.14:g.152660741T>C , CM000669.2:g.152660741T>C | GRCh38 |
NC_000007.13:g.152357826T>C , CM000669.1:g.152357826T>C | GRCh37 |
NC_000007.12:g.151988759T>C | NCBI36 |
NG_027988.1:g.20425A>G | |
NG_027988.2:g.20425A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000698506.1:c.-47-11378A>G | ENSP00000513758.1:n.-47-11378A>G | |
ENST00000698507.1:n.149A>G | ||
ENST00000359321.2:c.81A>G MANE Select | ENSP00000352271.1:p.Ile27Met | |
ENST00000359321.1:c.81A>G | ENSP00000352271.1:p.Ile27Met | |
ENST00000495707.1:n.103A>G | ||
NM_005431.1:c.81A>G | NP_005422.1:p.Ile27Met | |
NM_005431.2:c.81A>G MANE Select | NP_005422.1:p.Ile27Met |