HGVS | Genome Assembly |
---|---|
NC_000001.11:g.206116708C>G , CM000663.2:g.206116708C>G | GRCh38 |
NC_000001.10:g.206224623G>C , CM000663.1:g.206224623G>C | GRCh37 |
NC_000001.9:g.204391246G>C | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000367126.5:c.183G>C MANE Select | ENSP00000356094.4:p.Gln61His | |
ENST00000367126.4:c.183G>C | ENSP00000356094.4:p.Gln61His | |
ENST00000612906.1:n.36+956G>C | ||
NM_000707.3:c.183G>C | NP_000698.1:p.Gln61His | |
NM_000707.4:c.183G>C | NP_000698.1:p.Gln61His | |
NM_000707.5:c.183G>C MANE Select | NP_000698.1:p.Gln61His |