HGVS | Genome Assembly |
---|---|
NC_000001.11:g.171652569T>C , CM000663.2:g.171652569T>C | GRCh38 |
NC_000001.10:g.171621709T>C , CM000663.1:g.171621709T>C | GRCh37 |
NC_000001.9:g.169888332T>C | NCBI36 |
NG_008859.1:g.5065A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000037502.11:c.43A>G MANE Select | ENSP00000037502.5:p.Met15Val | |
ENST00000638471.1:c.43A>G | ENSP00000491206.1:p.Met15Val | |
ENST00000037502.10:c.43A>G | ENSP00000037502.5:p.Met15Val | |
ENST00000614688.1:c.43A>G | ENSP00000478680.1:p.Met15Val | |
NM_000261.1:c.43A>G | NP_000252.1:p.Met15Val | |
NM_000261.2:c.43A>G MANE Select | NP_000252.1:p.Met15Val |